SMART Health Cards: Vaccination & Testing Implementation Guide
1.0.0 - STU 1
SMART Health Cards: Vaccination & Testing Implementation Guide
1.0.0 - STU 1
SMART Health Cards: Vaccination & Testing Implementation Guide, published by HL7 International / Public Health. This guide is not an authorized publication; it is the continuous build for version 1.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-shc-vaccination-ig/ and changes regularly. See the Directory of published versions
| Official URL: http://hl7.org/fhir/uv/shc-vaccination/ValueSet/lab-result-findings | Version: 1.0.0 | |||
| Standards status: Trial-use | Maturity Level: 4 | Computable Name: LabResultFindings | ||
Copyright/Legal: This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement The SNOMED International IPS Terminology is distributed by International Health Terminology Standards Development Organisation, trading as SNOMED International, and is subject the terms of the Creative Commons Attribution 4.0 International Public License. For more information, see SNOMED IPS Terminology The HL7 International IPS implementation guides incorporate SNOMED CT®, used by permission of the International Health Terminology Standards Development Organisation, trading as SNOMED International. SNOMED CT was originally created by the College of American Pathologists. SNOMED CT is a registered trademark of the International Health Terminology Standards Development Organisation, all rights reserved. Implementers of SNOMED CT should review usage terms or directly contact SNOMED International: info@snomed.org |
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This value set includes SNOMED CT codes for identifying laboratory test results.
References
This value set includes codes based on the following rules:
http://snomed.info/sct version Not Stated (use latest from terminology server) where concept descends from 441742003 (Evaluation finding)http://snomed.info/sct version Not Stated (use latest from terminology server) where concept descends from 362981000 (Qualifier value)
Expansion from tx.fhir.org based on SNOMED CT International edition 01-Feb 2025
This value set has >1000 codes in it. In order to keep the publication size manageable, only a selection (1000 codes) of the whole set of codes is shown
| System | Code | Display (en) | JSON | XML |
http://snomed.info/sct | 183005 | Autoimmune pancytopenia | ||
http://snomed.info/sct | 292003 | EEG finding | ||
http://snomed.info/sct | 398002 | Left axis deviation greater than -90 degrees by EKG | ||
http://snomed.info/sct | 437009 | Abnormal composition of urine | ||
http://snomed.info/sct | 479003 | Graves' disease with pretibial myxedema AND with thyrotoxic crisis | ||
http://snomed.info/sct | 518002 | Multiple aggregation | ||
http://snomed.info/sct | 816009 | Genetic recombination | ||
http://snomed.info/sct | 827006 | Late congenital syphilis, latent (+ sero., - C.S.F., 2 years OR more) | ||
http://snomed.info/sct | 842009 | Consanguinity | ||
http://snomed.info/sct | 934007 | Thalassemia intermedia | ||
http://snomed.info/sct | 991002 | Wide QRS complex | ||
http://snomed.info/sct | 1077002 | Septal infarction by EKG | ||
http://snomed.info/sct | 1107004 | Early latent syphilis, positive serology, negative cerebrospinal fluid, with relapse after treatment (disorder) | ||
http://snomed.info/sct | 1152001 | Skin reaction negative | ||
http://snomed.info/sct | 1155004 | EKG hypertrophy | ||
http://snomed.info/sct | 1168007 | Allotype | ||
http://snomed.info/sct | 1318006 | Post-translational genetic protein processing | ||
http://snomed.info/sct | 1393001 | Lenz-Majewski hyperostosis syndrome | ||
http://snomed.info/sct | 1592005 | Failed attempted abortion with uremia | ||
http://snomed.info/sct | 1663004 | G2 stage | ||
http://snomed.info/sct | 1777007 | Increased molecular dissociation | ||
http://snomed.info/sct | 2243000 | Hypercalcemia due to hyperthyroidism | ||
http://snomed.info/sct | 2308003 | Silent alleles | ||
http://snomed.info/sct | 2351004 | Genetic transduction | ||
http://snomed.info/sct | 2388001 | Normal variation in translucency | ||
http://snomed.info/sct | 2398007 | Quinidine toxicity by EKG | ||
http://snomed.info/sct | 2634004 | Decreased blood erythrocyte volume | ||
http://snomed.info/sct | 2638001 | Drug-induced hypercalcaemia | ||
http://snomed.info/sct | 2657005 | Overflow proteinuria | ||
http://snomed.info/sct | 2663001 | Palpatory proteinuria | ||
http://snomed.info/sct | 2724004 | Recruitment | ||
http://snomed.info/sct | 2740001 | Gouty proteinuria | ||
http://snomed.info/sct | 2835000 | Traumatic cardiac hemolytic anemia | ||
http://snomed.info/sct | 2897005 | Thrombocytopenia due to immune destruction | ||
http://snomed.info/sct | 2902006 | Decreased lymphocyte life span | ||
http://snomed.info/sct | 2990008 | Lymphocytic leukemoid reaction | ||
http://snomed.info/sct | 3067005 | Blood group antigen C^u^ | ||
http://snomed.info/sct | 3391005 | Negative for tumor cells | ||
http://snomed.info/sct | 3720003 | Abnormal presence of hemoglobin | ||
http://snomed.info/sct | 3902000 | Non dose-related drug-induced neutropenia | ||
http://snomed.info/sct | 3909009 | Coeur en sabot | ||
http://snomed.info/sct | 3939004 | Bacterial colony density, transparent | ||
http://snomed.info/sct | 3947004 | High oxygen affinity hemoglobin polycythemia | ||
http://snomed.info/sct | 3978000 | Hemolytic anemia due to warm antibody | ||
http://snomed.info/sct | 4575002 | Acute hyponatremia | ||
http://snomed.info/sct | 4854004 | Acquired hemolytic anemia | ||
http://snomed.info/sct | 4939006 | Hemolytic anemia due to nonlymphoid neoplasm | ||
http://snomed.info/sct | 4984008 | Microcytic normochromic anemia | ||
http://snomed.info/sct | 5177007 | EKG axis finding | ||
http://snomed.info/sct | 5277004 | Urinary casts | ||
http://snomed.info/sct | 5300004 | Hemoglobin Bart's hydrops syndrome | ||
http://snomed.info/sct | 5315003 | Adenosine deaminase superactivity | ||
http://snomed.info/sct | 5523002 | Idiopathic myoglobinuria | ||
http://snomed.info/sct | 5559008 | Normal cellular morphology | ||
http://snomed.info/sct | 5603006 | Autoimmune hemolytic anemia caused by immunoglobulin G (disorder) | ||
http://snomed.info/sct | 5850000 | Suggest repeat smears | ||
http://snomed.info/sct | 5876000 | Acquired pancytopenia | ||
http://snomed.info/sct | 5967006 | A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis | ||
http://snomed.info/sct | 5994005 | Hereditary elliptocytosis due to deficiency of protein 4.1 | ||
http://snomed.info/sct | 6346007 | Leukocyte maturation arrest | ||
http://snomed.info/sct | 6390002 | Fine dispersion | ||
http://snomed.info/sct | 6398009 | Idiopathic chronic cold agglutinin disease | ||
http://snomed.info/sct | 6412007 | Digitalis toxicity by EKG | ||
http://snomed.info/sct | 6510002 | VX stage | ||
http://snomed.info/sct | 6631009 | Thrombocytosis | ||
http://snomed.info/sct | 6659005 | Megaloblastic anemia due to nontropical sprue | ||
http://snomed.info/sct | 6679002 | Specimen less than optimal for diagnosis | ||
http://snomed.info/sct | 6800004 | Blood group antigen E^u^ | ||
http://snomed.info/sct | 6907002 | Hemolysin factor | ||
http://snomed.info/sct | 7085002 | Hypercalcemia due to sarcoidosis | ||
http://snomed.info/sct | 7326005 | Inferior infarction by EKG | ||
http://snomed.info/sct | 7501002 | Increased lactic acid level | ||
http://snomed.info/sct | 7599007 | Genetic behavior | ||
http://snomed.info/sct | 7667005 | Specimen shows excessive cytolysis | ||
http://snomed.info/sct | 7705008 | Specimen inadequate for hormonal evaluation | ||
http://snomed.info/sct | 7724006 | Nephritic syndrome | ||
http://snomed.info/sct | 7766007 | Cloudy urine | ||
http://snomed.info/sct | 7923005 | Molecular cloning | ||
http://snomed.info/sct | 8022000 | Exercise proteinuria | ||
http://snomed.info/sct | 8116006 | Phenotype | ||
http://snomed.info/sct | 8399009 | Skin test reaction conversion | ||
http://snomed.info/sct | 8857001 | Hereditary elliptocytosis due to alpha spectrin defect | ||
http://snomed.info/sct | 8875000 | Colliquative proteinuria | ||
http://snomed.info/sct | 9109004 | Genetic alleles | ||
http://snomed.info/sct | 9111008 | Glucoglycinuria | ||
http://snomed.info/sct | 9123002 | Increased turbidity | ||
http://snomed.info/sct | 9147009 | Osteopoikilosis | ||
http://snomed.info/sct | 9426002 | Erythrocytosis due to hydronephrosis | ||
http://snomed.info/sct | 9437001 | Abnormal presence of myoglobin | ||
http://snomed.info/sct | 9723006 | Hyperphosphatasemia with bone disease | ||
http://snomed.info/sct | 9757003 | Delayed skin test reaction | ||
http://snomed.info/sct | 9872007 | Normal translucency | ||
http://snomed.info/sct | 10191004 | Anticoagulant effect | ||
http://snomed.info/sct | 10406007 | Lesch-Nyhan syndrome | ||
http://snomed.info/sct | 10564005 | Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin | ||
http://snomed.info/sct | 10589004 | Genetic transcription | ||
http://snomed.info/sct | 11109001 | Spontaneous abortion with uremia | ||
http://snomed.info/sct | 11187001 | Bacterial colony hemolysis, alpha prime | ||
http://snomed.info/sct | 11216008 | Fernandez reaction to lepromin | ||
http://snomed.info/sct | 11659006 | Uremic neuropathy | ||
http://snomed.info/sct | 11781007 | Autoimmune hemolytic anemia caused by complement | ||
http://snomed.info/sct | 11888009 | Hyperviscosity syndrome | ||
http://snomed.info/sct | 12178007 | Nephrogenous proteinuria | ||
http://snomed.info/sct | 12189000 | Coombs negative hemolytic anemia | ||
http://snomed.info/sct | 12531002 | Coarse dispersion | ||
http://snomed.info/sct | 12534005 | Unidentified pathogenic bacteria recovered | ||
http://snomed.info/sct | 12554006 | Laxity | ||
http://snomed.info/sct | 12645001 | Gene amplification | ||
http://snomed.info/sct | 12774002 | Bacterial colony morphology, entire margin | ||
http://snomed.info/sct | 12816000 | Bacterial colony size, large | ||
http://snomed.info/sct | 12907000 | Thiamine-responsive megaloblastic anemia | ||
http://snomed.info/sct | 13172003 | Chronic idiopathic thrombocytopenic purpura | ||
http://snomed.info/sct | 13300001 | Genetic linkage equilibrium | ||
http://snomed.info/sct | 13333006 | Genetic terminator region | ||
http://snomed.info/sct | 13465008 | Bacterial colony elevation, dome shaped | ||
http://snomed.info/sct | 13500002 | Electrocerebral silence | ||
http://snomed.info/sct | 13644009 | Hypercholesterolemia | ||
http://snomed.info/sct | 13703002 | No bacterial antibody increase, paired specimens | ||
http://snomed.info/sct | 13720003 | Triclonal gammopathy | ||
http://snomed.info/sct | 13930000 | Abnormal presence of protein | ||
http://snomed.info/sct | 14024008 | Humoral immunologic aplastic anemia | ||
http://snomed.info/sct | 14028006 | Abnormal thickness | ||
http://snomed.info/sct | 14087004 | Hereditary stomatocytosis | ||
http://snomed.info/sct | 14333004 | Alloimmune neonatal neutropenia | ||
http://snomed.info/sct | 14483005 | Coarse granular consistency | ||
http://snomed.info/sct | 14514008 | Anemia due to disturbance of hemoglobin synthesis | ||
http://snomed.info/sct | 14915001 | Gene dosage compensation | ||
http://snomed.info/sct | 15111002 | Pelger-Huët cell | ||
http://snomed.info/sct | 15121005 | Hereditary elliptocytosis due to glycophorin C deficiency | ||
http://snomed.info/sct | 15173006 | Rare organisms | ||
http://snomed.info/sct | 15212002 | Abnormal macromolecular binding | ||
http://snomed.info/sct | 15232001 | Increased vascular markings of lung | ||
http://snomed.info/sct | 15268006 | Abnormal presence of galactose | ||
http://snomed.info/sct | 15276008 | Drug-induced enzyme deficiency anemia | ||
http://snomed.info/sct | 15326009 | beta^+^ Thalassemia, normal Hb A>2<, type 2 | ||
http://snomed.info/sct | 15454001 | Increased size | ||
http://snomed.info/sct | 15466007 | Erythrocytosis due to cerebellar hemangioma | ||
http://snomed.info/sct | 15470004 | Toxic diffuse goiter with acropachy | ||
http://snomed.info/sct | 15656008 | Morphologic diagnosis deferred | ||
http://snomed.info/sct | 16021003 | Artifact due to freezing | ||
http://snomed.info/sct | 16289009 | Bacterial growth in animal culture | ||
http://snomed.info/sct | 16315008 | Depolymerization | ||
http://snomed.info/sct | 16345006 | Blood group antigen G^u^ | ||
http://snomed.info/sct | 16360009 | Delta-beta thalassemia | ||
http://snomed.info/sct | 16427007 | Delta thalassaemia | ||
http://snomed.info/sct | 16601003 | Bacterial colony consistency, viscous | ||
http://snomed.info/sct | 16618004 | Polyclonal gammopathy | ||
http://snomed.info/sct | 16964007 | Hereditary persistence of fetal hemoglobin thalassemia | ||
http://snomed.info/sct | 17221002 | Bacterial colony elevation, flat | ||
http://snomed.info/sct | 17235000 | Spherocytosis | ||
http://snomed.info/sct | 17342003 | Hereditary pure erythrocytosis | ||
http://snomed.info/sct | 17456000 | Breslow measurement - depth from 0.76 to 1.75 mm (finding) | ||
http://snomed.info/sct | 17523003 | Genetic mosaic | ||
http://snomed.info/sct | 17547005 | Thickening of vocal cords | ||
http://snomed.info/sct | 17928001 | Light-chain proteinuria | ||
http://snomed.info/sct | 18250007 | Decrease in circumference | ||
http://snomed.info/sct | 18259008 | EEG abnormality without seizure | ||
http://snomed.info/sct | 18273004 | Unstable hemoglobin disease | ||
http://snomed.info/sct | 18323000 | Innocent bystander type hemolytic anemia | ||
http://snomed.info/sct | 18565007 | Redistribution | ||
http://snomed.info/sct | 19281006 | Bacterial colony size | ||
http://snomed.info/sct | 19307009 | Drug-induced thrombocytopenic purpura | ||
http://snomed.info/sct | 19442009 | Heterozygous thalassemia | ||
http://snomed.info/sct | 19482002 | Regulatory sequence | ||
http://snomed.info/sct | 19539001 | Bacterial colony density | ||
http://snomed.info/sct | 19588001 | Erythrocytosis due to tissue hypoxemia | ||
http://snomed.info/sct | 19636003 | Monocytosis | ||
http://snomed.info/sct | 19730000 | Abnormally hard consistency | ||
http://snomed.info/sct | 19776001 | Decreased size | ||
http://snomed.info/sct | 19998002 | Megakaryocytic maturation arrest | ||
http://snomed.info/sct | 20329001 | Low ventricular voltage by EKG | ||
http://snomed.info/sct | 21412009 | X chromosome-linked pyridoxine refractory sideroblastic anemia | ||
http://snomed.info/sct | 21845002 | Granular consistency | ||
http://snomed.info/sct | 22061001 | Homozygote | ||
http://snomed.info/sct | 22098000 | Chronic idiopathic hemolytic anemia | ||
http://snomed.info/sct | 22310002 | Chronic idiopathic monocytosis | ||
http://snomed.info/sct | 22794007 | Hematogenous proteinuria | ||
http://snomed.info/sct | 22933009 | G-6-PD class I variant anemia | ||
http://snomed.info/sct | 22986007 | Transcriptional RNA splicing | ||
http://snomed.info/sct | 23132008 | AL amyloidosis | ||
http://snomed.info/sct | 23205009 | Transient neonatal thrombocytopenia | ||
http://snomed.info/sct | 23371004 | Epsilon gamma delta beta thalassemia | ||
http://snomed.info/sct | 23506009 | Normal flora | ||
http://snomed.info/sct | 23624004 | Bacterial colony surface, creamy | ||
http://snomed.info/sct | 23875004 | No pathologic diagnosis | ||
http://snomed.info/sct | 23891001 | Febrile proteinuria | ||
http://snomed.info/sct | 24052000 | Hypercalcemia due to immobilization | ||
http://snomed.info/sct | 24122006 | Inequality in circumference | ||
http://snomed.info/sct | 24129002 | Fasciitis with eosinophilia syndrome | ||
http://snomed.info/sct | 24159007 | Persistent lymphocytosis | ||
http://snomed.info/sct | 24390000 | Increased urobilinogen level | ||
http://snomed.info/sct | 24403008 | P-null phenotype | ||
http://snomed.info/sct | 24463005 | Asthenozoospermia | ||
http://snomed.info/sct | 24480009 | Abnormal nerve conduction | ||
http://snomed.info/sct | 24620004 | Hemolytic anemia due to babesiosis | ||
http://snomed.info/sct | 24652004 | Decreased markings | ||
http://snomed.info/sct | 24661004 | G-6-PD class III variant anemia | ||
http://snomed.info/sct | 24752008 | Infantile cortical hyperostosis | ||
http://snomed.info/sct | 24829000 | Eosinophilic ulcerative colitis | ||
http://snomed.info/sct | 24942001 | Urobilinogenuria | ||
http://snomed.info/sct | 24974008 | Myelokathexis | ||
http://snomed.info/sct | 24975009 | Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin | ||
http://snomed.info/sct | 25050002 | Alpha heavy chain disease, respiratory form | ||
http://snomed.info/sct | 25132006 | Blood group N>2< | ||
http://snomed.info/sct | 25194005 | Abnormal nucleotide base sequence | ||
http://snomed.info/sct | 25251008 | HNSHA due to gamma glutamyl cysteine synthetase deficiency | ||
http://snomed.info/sct | 25266006 | Hereditary spherocytosis due to spectrin deficiency | ||
http://snomed.info/sct | 25363001 | Genetic non disjunction | ||
http://snomed.info/sct | 25384006 | Blood group S>2< | ||
http://snomed.info/sct | 25443007 | X chromosome-linked pyridoxine responsive sideroblastic anemia | ||
http://snomed.info/sct | 25488008 | Left ventricular hypertrophy by EKG | ||
http://snomed.info/sct | 25502009 | Episodic lymphocytopenia | ||
http://snomed.info/sct | 25601009 | Erythrocytosis due to autotransfusion | ||
http://snomed.info/sct | 25778006 | Bacterial colony consistency, butyrous | ||
http://snomed.info/sct | 25881005 | High altitude polycythemia | ||
http://snomed.info/sct | 25900007 | Gene re-arrangement, B lymphocyte, heavy chain | ||
http://snomed.info/sct | 26141007 | ST segment depression | ||
http://snomed.info/sct | 26151008 | Graves' disease with acropachy AND with thyrotoxic crisis | ||
http://snomed.info/sct | 26165005 | Increased bilirubin level | ||
http://snomed.info/sct | 26298008 | Diabetic coma with ketoacidosis | ||
http://snomed.info/sct | 26389007 | Toxic multinodular goiter | ||
http://snomed.info/sct | 26409005 | Congenital dyserythropoietic anemia, type III | ||
http://snomed.info/sct | 26489008 | Bacterial colony surface appearance | ||
http://snomed.info/sct | 26576000 | Positive skin test reaction | ||
http://snomed.info/sct | 26608005 | Carbohydrate sequence | ||
http://snomed.info/sct | 26682008 | Homozygous beta thalassemia | ||
http://snomed.info/sct | 26875006 | Bacterial colony elevation, convex | ||
http://snomed.info/sct | 26944003 | Acute megaloblastic anemia due to dialysis | ||
http://snomed.info/sct | 27080008 | Beta zero thalassemia deletion type | ||
http://snomed.info/sct | 27396000 | Cathodal opening clonus | ||
http://snomed.info/sct | 27649004 | Left ventricular S-T changes | ||
http://snomed.info/sct | 27798002 | Megaloblastic anemia due to impaired absorption of folate | ||
http://snomed.info/sct | 27837003 | Pyle metaphyseal dysplasia | ||
http://snomed.info/sct | 27863008 | No organisms seen | ||
http://snomed.info/sct | 27868004 | Chronic steatorrhea | ||
http://snomed.info/sct | 28147001 | Haemolytic anaemia caused by Clostridium welchii | ||
http://snomed.info/sct | 28166001 | Molecular degradation | ||
http://snomed.info/sct | 28319009 | Erythrocytosis due to cardiovascular disease | ||
http://snomed.info/sct | 28328005 | Radiologic markings | ||
http://snomed.info/sct | 28630001 | Shortened QRS complex | ||
http://snomed.info/sct | 28798000 | Substance not assigned to a scientific category | ||
http://snomed.info/sct | 28820008 | Amino acid sequence | ||
http://snomed.info/sct | 28965003 | Deficiency of DNA repair | ||
http://snomed.info/sct | 28975000 | Constitutional aplastic anemia | ||
http://snomed.info/sct | 29082008 | Normal stimulus response of nerve cell and nerve fiber | ||
http://snomed.info/sct | 29120000 | Eosinophilic colitis | ||
http://snomed.info/sct | 29177004 | Anemia due to pentose phosphate pathway defect | ||
http://snomed.info/sct | 29230002 | Bacterial growth in artificial medium | ||
http://snomed.info/sct | 29286002 | Abnormal nucleic acid sequence | ||
http://snomed.info/sct | 29489007 | EKG axis perpendicular to frontal plane | ||
http://snomed.info/sct | 29549004 | RRNA operon | ||
http://snomed.info/sct | 29738008 | Proteinuria | ||
http://snomed.info/sct | 29746009 | Normal distribution | ||
http://snomed.info/sct | 29789008 | Monocytic leukemoid reaction | ||
http://snomed.info/sct | 30182008 | Thrombocytopenia due to extracorporeal circulation (disorder) | ||
http://snomed.info/sct | 30257002 | Abnormal fibrinolysis | ||
http://snomed.info/sct | 30271005 | Bacterial colony surface, granular | ||
http://snomed.info/sct | 30389008 | Normal tissue | ||
http://snomed.info/sct | 30453001 | Abnormal molecular cross-linking | ||
http://snomed.info/sct | 30575002 | Fanconi pancytopenia syndrome | ||
http://snomed.info/sct | 30981000 | Secondary eosinophilia | ||
http://snomed.info/sct | 30985009 | Toxic nodular goiter with thyrotoxic storm | ||
http://snomed.info/sct | 31091003 | Sister chromatid exchange | ||
http://snomed.info/sct | 31137003 | Early latent syphilis, positive serology, negative cerebrospinal fluid, less than 2 years after infection (disorder) | ||
http://snomed.info/sct | 31153000 | Bacterial colony shape, filamentous | ||
http://snomed.info/sct | 31563000 | Asymptomatic bacteriuria in pregnancy | ||
http://snomed.info/sct | 31649001 | Abnormal presence of glucose | ||
http://snomed.info/sct | 31991001 | Leukocytic phagocytosis | ||
http://snomed.info/sct | 32092008 | Toxic neutropenia | ||
http://snomed.info/sct | 32475006 | F>2< generation | ||
http://snomed.info/sct | 32482005 | Orthostatic proteinuria | ||
http://snomed.info/sct | 32648007 | Mild hereditary spherocytosis due to spectrin deficiency | ||
http://snomed.info/sct | 32775005 | Indeterminate axis by EKG | ||
http://snomed.info/sct | 32855007 | HPFH unlinked to beta-globulin gene cluster | ||
http://snomed.info/sct | 32858009 | Hemolytic disease of fetus OR newborn due to ABO immunization | ||
http://snomed.info/sct | 32984002 | Neonatal polycythemia | ||
http://snomed.info/sct | 33002009 | Macromolecular defective synthesis | ||
http://snomed.info/sct | 33033006 | March myoglobinuria | ||
http://snomed.info/sct | 33054004 | Polymerization | ||
http://snomed.info/sct | 33183004 | Post infectious thrombocytopenic purpura | ||
http://snomed.info/sct | 33419001 | LX stage | ||
http://snomed.info/sct | 33491002 | Autoimmune hemolytic anemia caused by IgA plus complement | ||
http://snomed.info/sct | 33513003 | Familial apolipoprotein C-II deficiency | ||
http://snomed.info/sct | 33779007 | Bacterial antibody present | ||
http://snomed.info/sct | 33905008 | Hereditary spherocytosis due to deficiency of protein 4.2 | ||
http://snomed.info/sct | 34165000 | Gestational proteinuria | ||
http://snomed.info/sct | 34194007 | HNSHA due to pyrimidine-5'-nucleotidase deficiency | ||
http://snomed.info/sct | 34216002 | Proposita | ||
http://snomed.info/sct | 34225008 | Idiopathic hypercalcemia of infancy | ||
http://snomed.info/sct | 34247008 | Anemia due to mechanical damage | ||
http://snomed.info/sct | 34327003 | Parturient hemorrhage associated with hyperfibrinolysis | ||
http://snomed.info/sct | 34349009 | Familial type 5 hyperlipoproteinemia | ||
http://snomed.info/sct | 34395002 | Thrombocytopenia due to hypothermia | ||
http://snomed.info/sct | 34397005 | Erythrocytosis due to uterine myoma | ||
http://snomed.info/sct | 34528009 | Familial hypertriglyceridemia | ||
http://snomed.info/sct | 34643004 | Diaphyseal dysplasia | ||
http://snomed.info/sct | 34782005 | Chromosomal inheritance | ||
http://snomed.info/sct | 34850003 | Blood group antigen Fy^x^ | ||
http://snomed.info/sct | 34852006 | G-6-PD class II variant anemia | ||
http://snomed.info/sct | 34875004 | Bacterial colony elevation, raised | ||
http://snomed.info/sct | 34898007 | Bacterial colony morphology | ||
http://snomed.info/sct | 34925000 | Megaloblastic anemia due to inborn errors of metabolism | ||
http://snomed.info/sct | 34993002 | Mixed proteinuria | ||
http://snomed.info/sct | 35010007 | Cathodal closure clonus | ||
http://snomed.info/sct | 35147005 | Genetic crossing over | ||
http://snomed.info/sct | 35357002 | Bacterial colony morphology, margin | ||
http://snomed.info/sct | 35508004 | Empty delta sign | ||
http://snomed.info/sct | 35703006 | Transient paroxysmal cold hemoglobinuria | ||
http://snomed.info/sct | 35727008 | Cardiac proteinuria | ||
http://snomed.info/sct | 35778001 | Megaloblastic anemia due to error of folate metabolism | ||
http://snomed.info/sct | 35868009 | Carcinoid syndrome | ||
http://snomed.info/sct | 35885006 | Hyperuricemia | ||
http://snomed.info/sct | 35912001 | Aminoaciduria | ||
http://snomed.info/sct | 36070007 | Wiskott-Aldrich syndrome | ||
http://snomed.info/sct | 36222008 | Carcinoid heart disease | ||
http://snomed.info/sct | 36241006 | Non-toxic multinodular goiter | ||
http://snomed.info/sct | 36350006 | Abnormally soft consistency | ||
http://snomed.info/sct | 36351005 | Antithrombin III deficiency | ||
http://snomed.info/sct | 36467003 | Alpha plus thalassemia | ||
http://snomed.info/sct | 36472007 | Hemoglobin S-F disease | ||
http://snomed.info/sct | 36506006 | Normal thickness | ||
http://snomed.info/sct | 36568005 | Hemolytic uremic syndrome of childhood | ||
http://snomed.info/sct | 36580002 | Bacterial colony morphology, lobate margin | ||
http://snomed.info/sct | 36597008 | Molecular dissociation | ||
http://snomed.info/sct | 36601008 | Craniometaphyseal dysplasia | ||
http://snomed.info/sct | 36815008 | Acetonuria | ||
http://snomed.info/sct | 36874002 | Stress polycythemia | ||
http://snomed.info/sct | 36898009 | Friability | ||
http://snomed.info/sct | 36919001 | Anemia caused by lead | ||
http://snomed.info/sct | 37097005 | Erythroblastosis | ||
http://snomed.info/sct | 37253000 | Decreased osmotic fragility | ||
http://snomed.info/sct | 37398008 | Diabetic urine | ||
http://snomed.info/sct | 37447003 | Substance type not applicable | ||
http://snomed.info/sct | 37492005 | Sex-linked thrombocytopenia | ||
http://snomed.info/sct | 37558005 | Abnormal saltatory conduction | ||
http://snomed.info/sct | 37774003 | Bacterial colony hemolysis | ||
http://snomed.info/sct | 37794007 | Retraction | ||
http://snomed.info/sct | 37819008 | Genetic sequence homology | ||
http://snomed.info/sct | 38064006 | Reactive monocytosis | ||
http://snomed.info/sct | 38194003 | Blood group antigen e^i^ | ||
http://snomed.info/sct | 38531000 | Diminished LV forces by EKG | ||
http://snomed.info/sct | 38638004 | Increased translucency | ||
http://snomed.info/sct | 38689004 | Hemolytic anemia due to infection | ||
http://snomed.info/sct | 38697006 | Polycythemia due to donor twin transfusion | ||
http://snomed.info/sct | 38789009 | Genetic dosage effect | ||
http://snomed.info/sct | 38911009 | Hereditary hemolytic anemia | ||
http://snomed.info/sct | 38970002 | Doan-Wright syndrome | ||
http://snomed.info/sct | 39090004 | Bacterial colony size, small | ||
http://snomed.info/sct | 39112005 | Glutathione synthase deficiency with 5-oxoprolinuria | ||
http://snomed.info/sct | 39321000 | Shadow | ||
http://snomed.info/sct | 39586009 | HPFH A gamma beta^+^ thalassemia | ||
http://snomed.info/sct | 39696006 | Bacterial colony shape, irregular | ||
http://snomed.info/sct | 39732003 | Left axis deviation | ||
http://snomed.info/sct | 39751009 | Genetic position effect | ||
http://snomed.info/sct | 39841003 | Normal consistency | ||
http://snomed.info/sct | 40108008 | Thalassemia | ||
http://snomed.info/sct | 40223008 | V0 stage | ||
http://snomed.info/sct | 40233000 | Nephrotic-nephritic syndrome | ||
http://snomed.info/sct | 40241000 | Denaturation | ||
http://snomed.info/sct | 40387008 | Polyagglutinable erythrocyte syndrome | ||
http://snomed.info/sct | 40434009 | Dyspeptic urine | ||
http://snomed.info/sct | 40679002 | Erythrocytosis due to alveolar hypoventilation | ||
http://snomed.info/sct | 40976007 | Genetic linkage disequilibrium | ||
http://snomed.info/sct | 41350008 | Decreased granulocyte life span | ||
http://snomed.info/sct | 41387000 | HNSHA due to phosphofructokinase deficiency | ||
http://snomed.info/sct | 41405005 | Muscle fibrillation | ||
http://snomed.info/sct | 41482005 | Molecular sequence data | ||
http://snomed.info/sct | 41614006 | Hypoplastic anemia | ||
http://snomed.info/sct | 41716002 | Light-induced EEG abnormality | ||
http://snomed.info/sct | 41814009 | Neutropenia with dysgranulopoiesis | ||
http://snomed.info/sct | 41835006 | Reaction of denervation by electromyogram | ||
http://snomed.info/sct | 41934009 | Analysis for substance type not performed | ||
http://snomed.info/sct | 42484009 | HNSHA due to hexokinase deficiency | ||
http://snomed.info/sct | 42601008 | Congenital hemolytic anemia | ||
http://snomed.info/sct | 42616006 | Erythrocytosis due to hepatoma | ||
http://snomed.info/sct | 42669007 | Hyponatremia with excess extracellular fluid volume | ||
http://snomed.info/sct | 42827006 | Globular proteinuria | ||
http://snomed.info/sct | 42844005 | Bacterial colony morphology, filamentous margin | ||
http://snomed.info/sct | 42852008 | Infectious lymphocytosis | ||
http://snomed.info/sct | 42959003 | Flare reaction | ||
http://snomed.info/sct | 43245005 | Gene re-arrangement | ||
http://snomed.info/sct | 43258006 | Milk alkali syndrome | ||
http://snomed.info/sct | 43355006 | Eosinopenia | ||
http://snomed.info/sct | 43376001 | Multiple alleles | ||
http://snomed.info/sct | 43400009 | EEG abnormality with seizure | ||
http://snomed.info/sct | 43468004 | Filling defect | ||
http://snomed.info/sct | 43515008 | Specimen not representative of anatomic site | ||
http://snomed.info/sct | 43630006 | Anterolateral infarction by EKG | ||
http://snomed.info/sct | 43707008 | Anemia caused by heat (disorder) | ||
http://snomed.info/sct | 43771008 | Morphology not applicable | ||
http://snomed.info/sct | 43820004 | Postrenal proteinuria | ||
http://snomed.info/sct | 43858000 | Secondary aplastic anemia | ||
http://snomed.info/sct | 43918003 | Erythrocytosis due to renal tumor | ||
http://snomed.info/sct | 43996000 | Nucleic acid conformation | ||
http://snomed.info/sct | 44206008 | Hapten type low affinity hemolytic anemia | ||
http://snomed.info/sct | 44288006 | Anemia due to extrinsic red cell abnormality | ||
http://snomed.info/sct | 44325009 | Diminished RV forces by EKG | ||
http://snomed.info/sct | 44371002 | Mixed polyclonal cryoimmunoglobulinemia | ||
http://snomed.info/sct | 44456000 | Inappropriate secondary erythrocytosis | ||
http://snomed.info/sct | 44641000 | HNSHA due to triosephosphate isomerase deficiency | ||
http://snomed.info/sct | 44649003 | L0 stage | ||
http://snomed.info/sct | 44666001 | Microcytic hypochromic anemia | ||
http://snomed.info/sct | 44697002 | Melorheostosis | ||
http://snomed.info/sct | 44724006 | Abnormal distribution | ||
http://snomed.info/sct | 44730006 | Uremia | ||
http://snomed.info/sct | 44734002 | Bacterial colony consistency, brittle | ||
http://snomed.info/sct | 44815009 | Breslow measurement - depth greater than 1.75 mm (finding) | ||
http://snomed.info/sct | 44832008 | Increase in circumference | ||
http://snomed.info/sct | 44865000 | Secondary polycythemia | ||
http://snomed.info/sct | 44880006 | Decreased macromolecular binding | ||
http://snomed.info/sct | 44998009 | Right ventricular S-T changes | ||
http://snomed.info/sct | 45113005 | Substance not assigned code in SNOMED | ||
http://snomed.info/sct | 45154002 | Glycosuria | ||
http://snomed.info/sct | 45212007 | F>1< generation | ||
http://snomed.info/sct | 45280006 | Bacterial colony surface, glistening | ||
http://snomed.info/sct | 45427005 | Hybrid vigor | ||
http://snomed.info/sct | 45597001 | Blood group A>3<B | ||
http://snomed.info/sct | 45646000 | Subacute milk alkali syndrome | ||
http://snomed.info/sct | 45670001 | Bacterial colony hemolysis, gamma | ||
http://snomed.info/sct | 45803000 | Genetic promotor region | ||
http://snomed.info/sct | 45841007 | Kappa light chain disease | ||
http://snomed.info/sct | 46049004 | Reticulocytosis | ||
http://snomed.info/sct | 46235002 | Early latent congenital syphilis, positive serology, negative spinal fluid (disorder) | ||
http://snomed.info/sct | 46359005 | Neutropenia associated with infectious disease | ||
http://snomed.info/sct | 46503001 | Negative for recurrent tumor | ||
http://snomed.info/sct | 46760003 | Estren-Dameshek anemia | ||
http://snomed.info/sct | 46784006 | Crystalluria | ||
http://snomed.info/sct | 46785007 | Familial juvenile gout | ||
http://snomed.info/sct | 47047009 | Thalassemia with other hemoglobinopathy | ||
http://snomed.info/sct | 47084006 | Beta plus thalassemia normal hemoglobin A>2< type 1 silent (disorder) | ||
http://snomed.info/sct | 47100003 | Anemia of prematurity | ||
http://snomed.info/sct | 47144000 | Acute neutrophilia | ||
http://snomed.info/sct | 47286004 | Aggregation | ||
http://snomed.info/sct | 47318007 | Drug-induced neutropenia | ||
http://snomed.info/sct | 47516005 | Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin | ||
http://snomed.info/sct | 47526003 | HNSHA due to NADH diaphorase deficiency | ||
http://snomed.info/sct | 47665007 | Right axis deviation | ||
http://snomed.info/sct | 47708004 | Genetic predisposition | ||
http://snomed.info/sct | 47709007 | Humoral hypercalcemia of malignancy | ||
http://snomed.info/sct | 47739002 | Myelophthisis | ||
http://snomed.info/sct | 47740000 | Bacterial colony surface, dull | ||
http://snomed.info/sct | 47872005 | Hypoviscosity | ||
http://snomed.info/sct | 47973001 | Artifact | ||
http://snomed.info/sct | 47986005 | Genetic anomaly of leukocyte | ||
http://snomed.info/sct | 48160003 | Lordotic proteinuria | ||
http://snomed.info/sct | 48165008 | Myoglobinuria | ||
http://snomed.info/sct | 48188009 | Azoospermia | ||
http://snomed.info/sct | 48250002 | Gaisbock's syndrome | ||
http://snomed.info/sct | 48408000 | Bacterial colony morphology, undulate margin | ||
http://snomed.info/sct | 48516007 | Acute infectious lymphocytosis | ||
http://snomed.info/sct | 48553001 | Hemoglobin H disease | ||
http://snomed.info/sct | 48744006 | Normal variation in thickness | ||
http://snomed.info/sct | 48788004 | Cyclic thrombocytopenia | ||
http://snomed.info/sct | 48796009 | Congenital nephrotic syndrome | ||
http://snomed.info/sct | 48813009 | Lymphocytopenia | ||
http://snomed.info/sct | 48883003 | Specimen satisfactory for diagnosis | ||
http://snomed.info/sct | 48983004 | X chromosome-linked sideroblastic anemia | ||
http://snomed.info/sct | 49030004 | Strand breaks | ||
http://snomed.info/sct | 49099001 | Increased uric acid level | ||
http://snomed.info/sct | 49284006 | Juvenile type megaloblastic anemia | ||
http://snomed.info/sct | 49578007 | Shortened PR interval | ||
http://snomed.info/sct | 49621008 | Gouty urine | ||
http://snomed.info/sct | 49886003 | Thrombocytopenia due to blood loss | ||
http://snomed.info/sct | 50004001 | No substance type identified | ||
http://snomed.info/sct | 50029007 | Familial hypomagnesemia-hypercalciuria | ||
http://snomed.info/sct | 50064003 | V2 stage | ||
http://snomed.info/sct | 50110003 | No endocervical cells present | ||
http://snomed.info/sct | 50220002 | Cellular immunologic aplastic anemia | ||
http://snomed.info/sct | 50253007 | Secondary paroxysmal cold hemoglobinuria | ||
http://snomed.info/sct | 50296002 | Lipid conformation | ||
http://snomed.info/sct | 50311009 | Erythrocyte aggregation | ||
http://snomed.info/sct | 50327002 | Chronic hyponatremia | ||
http://snomed.info/sct | 50334000 | Genetic polymorphism | ||
http://snomed.info/sct | 50551008 | Right shift of WBC | ||
http://snomed.info/sct | 50606000 | Genetic selection | ||
http://snomed.info/sct | 50715003 | Pure red cell aplasia | ||
http://snomed.info/sct | 50820005 | Cytopenia | ||
http://snomed.info/sct | 50935005 | Milky urine | ||
http://snomed.info/sct | 51028009 | Abnormal presence of pentose | ||
http://snomed.info/sct | 51071000 | Microangiopathic hemolytic anemia | ||
http://snomed.info/sct | 51183001 | Untoward skin test reaction | ||
http://snomed.info/sct | 51291001 | Negative for residual tumor | ||
http://snomed.info/sct | 51319002 | Light chain disease | ||
http://snomed.info/sct | 51381009 | Increased diameter | ||
http://snomed.info/sct | 51512005 | Nucleic acid repetitive sequence | ||
http://snomed.info/sct | 51624005 | Dilutional thrombocytopenia | ||
http://snomed.info/sct | 51798006 | Decreased glucose level | ||
http://snomed.info/sct | 51982005 | Emulsification | ||
http://snomed.info/sct | 52064007 | Biclonal gammopathy | ||
http://snomed.info/sct | 52212006 | HNSHA due to glutathione reductase deficiency | ||
http://snomed.info/sct | 52254009 | Nephrotic syndrome | ||
http://snomed.info/sct | 52413004 | HNSHA due to glucose phosphate isomerase deficiency | ||
http://snomed.info/sct | 52691008 | No microscopic confirmation - clinically metastatic tumor (cancer) | ||
http://snomed.info/sct | 52760008 | Hypercalcemia due to granulomatous disease | ||
http://snomed.info/sct | 52816004 | Genetic transactivation | ||
http://snomed.info/sct | 52828007 | Macromolecular alteration | ||
http://snomed.info/sct | 52842004 | Decreased turbidity | ||
http://snomed.info/sct | 52951008 | Congenital dyserythropoietic anemia | ||
http://snomed.info/sct | 52976009 | Sensitized cell | ||
http://snomed.info/sct | 53311008 | Normal variation in size | ||
http://snomed.info/sct | 53358000 | F factor | ||
http://snomed.info/sct | 53397008 | Biliuria | ||
http://snomed.info/sct | 53461003 | Normal size | ||
http://snomed.info/sct | 53586009 | Macromolecular binding | ||
http://snomed.info/sct | 53743006 | Anemia following fetal blood loss | ||
http://snomed.info/sct | 54006005 | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | ||
http://snomed.info/sct | 54079004 | Anodal opening clonus | ||
http://snomed.info/sct | 54082009 | Bacterial growth in cell culture | ||
http://snomed.info/sct | 54102005 | G1 stage | ||
http://snomed.info/sct | 54192004 | Specimen obscured by foreign material | ||
http://snomed.info/sct | 54236009 | Genetic replication | ||
http://snomed.info/sct | 54569005 | Bernard Soulier syndrome | ||
http://snomed.info/sct | 54665006 | Bacterial colony size, medium | ||
http://snomed.info/sct | 54828006 | Nucleotide base sequence | ||
http://snomed.info/sct | 55182004 | Surgical margins free of tumor | ||
http://snomed.info/sct | 55257005 | Wrong tissue received | ||
http://snomed.info/sct | 55444004 | Transient neonatal neutropenia | ||
http://snomed.info/sct | 55446002 | Genetic mutation | ||
http://snomed.info/sct | 55662002 | Enterogenic proteinuria | ||
http://snomed.info/sct | 55699002 | Bacterial colony shape, punctiform | ||
http://snomed.info/sct | 55759009 | Increase of specific gravity | ||
http://snomed.info/sct | 55822004 | Hyperlipidemia | ||
http://snomed.info/sct | 55907008 | Acquired aplastic anemia | ||
http://snomed.info/sct | 55930002 | S-T changes | ||
http://snomed.info/sct | 55995005 | Hereditary spherocytosis | ||
http://snomed.info/sct | 56205004 | HPFH nondeletion type | ||
http://snomed.info/sct | 56260006 | Prolonged ST segment | ||
http://snomed.info/sct | 56478004 | Leukemoid reaction | ||
http://snomed.info/sct | 56709009 | Target cell of immunologic reaction | ||
http://snomed.info/sct | 56879003 | Genetic independent segregation | ||
http://snomed.info/sct | 56918001 | Dose-related drug-induced neutropenia | ||
http://snomed.info/sct | 57009009 | Functional proteinuria | ||
http://snomed.info/sct | 57104001 | Finding related to response to skin test | ||
http://snomed.info/sct | 57160007 | Felty's syndrome | ||
http://snomed.info/sct | 57192008 | Acute pure red cell aplasia | ||
http://snomed.info/sct | 57196006 | Gene frequency | ||
http://snomed.info/sct | 57390009 | Mixed cryoimmunoglobulinemia with monoclonal component | ||
http://snomed.info/sct | 57557005 | Chronic milk alkali syndrome | ||
http://snomed.info/sct | 57652005 | Blood group antigen V^u^ | ||
http://snomed.info/sct | 57722009 | Sensitized red cell | ||
http://snomed.info/sct | 57777000 | Toxic nodular goiter | ||
http://snomed.info/sct | 58136006 | Nutritional disorder due to calcium-phosphorus imbalance | ||
http://snomed.info/sct | 58178000 | Tissue lost in processing | ||
http://snomed.info/sct | 58460004 | Blood group O | ||
http://snomed.info/sct | 58468006 | Colicin factor | ||
http://snomed.info/sct | 58648008 | Benign monoclonal gammopathy | ||
http://snomed.info/sct | 58899004 | No evidence of neoplasm | ||
http://snomed.info/sct | 59178007 | Menkes kinky-hair syndrome | ||
http://snomed.info/sct | 59462000 | Decreased EKG voltage | ||
http://snomed.info/sct | 59548005 | Congenital dyserythropoietic anemia, type I | ||
http://snomed.info/sct | 59614000 | Occult blood in stool | ||
http://snomed.info/sct | 59635003 | No microscopic confirmation - clinically tumor | ||
http://snomed.info/sct | 59644002 | HNSHA due to phosphoglycerate kinase deficiency | ||
http://snomed.info/sct | 59763006 | Hyperphosphatasemia tarda | ||
http://snomed.info/sct | 59828008 | Hemolytic crisis | ||
http://snomed.info/sct | 59931005 | Inverted T wave | ||
http://snomed.info/sct | 59957008 | Neonatal Graves' disease | ||
http://snomed.info/sct | 60164003 | Megaloblastic anemia due to blind loop syndrome | ||
http://snomed.info/sct | 60181007 | Allelic exclusion | ||
http://snomed.info/sct | 60216004 | Toxic diffuse goiter with thyrotoxic crisis | ||
http://snomed.info/sct | 60268006 | Toxic diffuse goiter with pretibial myxedema | ||
http://snomed.info/sct | 60399005 | Dermatofibrosis lenticularis disseminata | ||
http://snomed.info/sct | 60504009 | Megaloblastic anemia due to congenital deficiency of intrinsic factor | ||
http://snomed.info/sct | 60628003 | Mediterranean macrothrombocytopenia | ||
http://snomed.info/sct | 60805002 | Hemolytic anemia with emphysema AND cutis laxa | ||
http://snomed.info/sct | 60815008 | Grade not determined | ||
http://snomed.info/sct | 60844005 | Genetic inversion | ||
http://snomed.info/sct | 61026006 | G3 stage | ||
http://snomed.info/sct | 61037007 | Colloid goiter | ||
http://snomed.info/sct | 61070002 | Erythrophagocytosis | ||
http://snomed.info/sct | 61135002 | Residual proteinuria | ||
http://snomed.info/sct | 61261009 | Hemolytic anemia | ||
http://snomed.info/sct | 61373006 | Bacteriuria | ||
http://snomed.info/sct | 61395005 | Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | ||
http://snomed.info/sct | 61493004 | Mu heavy chain disease | ||
http://snomed.info/sct | 61596005 | Heterophil-positive mononucleosis syndrome | ||
http://snomed.info/sct | 61609004 | Gram-positive cocci in chains | ||
http://snomed.info/sct | 61668005 | Gene re-arrangement, gamma chain, T cell antigen receptor | ||
http://snomed.info/sct | 61721007 | Counterclockwise vectorcardiographic loop | ||
http://snomed.info/sct | 61744005 | Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia | ||
http://snomed.info/sct | 61777009 | Hemoglobin C-F disease | ||
http://snomed.info/sct | 61828008 | Lysogeny | ||
http://snomed.info/sct | 62074008 | Delta zero thalassemia (disorder) | ||
http://snomed.info/sct | 62117008 | Bacterial antibody increase, paired specimens | ||
http://snomed.info/sct | 62268000 | HNSHA due to diphosphoglycerate mutase deficiency | ||
http://snomed.info/sct | 62278002 | Toxic multinodular goiter with thyrotoxic crisis | ||
http://snomed.info/sct | 62403005 | Glucose-6-phosphate dehydrogenase deficiency anemia | ||
http://snomed.info/sct | 62410004 | Postpartum fibrinolysis with hemorrhage | ||
http://snomed.info/sct | 62609001 | Autoimmune haemolytic anaemia caused by immunoglobulin G plus complement | ||
http://snomed.info/sct | 62781006 | Increased platelet destruction | ||
http://snomed.info/sct | 62803002 | Frontometaphyseal dysplasia | ||
http://snomed.info/sct | 62871001 | Idiopathic paroxysmal cold hemoglobinuria | ||
http://snomed.info/sct | 62938001 | Normal strength-duration relationship of nerve cell and nerve fiber | ||
http://snomed.info/sct | 63038006 | Specimen obscured by inflammation | ||
http://snomed.info/sct | 63092005 | Immediate skin test reaction | ||
http://snomed.info/sct | 63192007 | Decreased uric acid level | ||
http://snomed.info/sct | 63325007 | Molecular aggregation | ||
http://snomed.info/sct | 63444004 | Thrombocytopenia due to hypersplenism | ||
http://snomed.info/sct | 63484008 | Drug-induced neutrophilia | ||
http://snomed.info/sct | 63565007 | Congenital anemia | ||
http://snomed.info/sct | 63583004 | Solitary aggregation | ||
http://snomed.info/sct | 63672004 | Absent skin test reaction | ||
http://snomed.info/sct | 63693001 | Genetic transformation | ||
http://snomed.info/sct | 63919000 | R factor | ||
http://snomed.info/sct | 64088006 | Hyperviscosity | ||
http://snomed.info/sct | 64195000 | Genetic variation | ||
http://snomed.info/sct | 64245008 | Propositus | ||
http://snomed.info/sct | 64249002 | Allergic eosinophilia | ||
http://snomed.info/sct | 64553001 | Secretor gene absent (se) | ||
http://snomed.info/sct | 64668006 | Sensitized leukocyte | ||
http://snomed.info/sct | 64781005 | Bacterial colony shape, circular | ||
http://snomed.info/sct | 64936001 | Löffler's syndrome | ||
http://snomed.info/sct | 64970000 | Substance type unknown | ||
http://snomed.info/sct | 65087006 | Blood group M>2< | ||
http://snomed.info/sct | 65113001 | DNA repair | ||
http://snomed.info/sct | 65209002 | Basophilia | ||
http://snomed.info/sct | 65230006 | Heterophil-negative mononucleosis syndrome | ||
http://snomed.info/sct | 65247007 | Gene re-arrangement, T lymphocyte | ||
http://snomed.info/sct | 65264005 | Macromolecular nicking | ||
http://snomed.info/sct | 65277001 | Imidazole aminoaciduria | ||
http://snomed.info/sct | 65476007 | Abnormal size | ||
http://snomed.info/sct | 65533007 | Sensitized platelet | ||
http://snomed.info/sct | 65623009 | Immune neutropenia | ||
http://snomed.info/sct | 65712000 | No microscopic confirmation - clinically benign tumor | ||
http://snomed.info/sct | 65783004 | Conjugative plasmid | ||
http://snomed.info/sct | 65798002 | Molecular cross-linking | ||
http://snomed.info/sct | 65959000 | Beta thalassemia | ||
http://snomed.info/sct | 66055002 | Alpha zero thalassemia | ||
http://snomed.info/sct | 66115002 | Molecular instability | ||
http://snomed.info/sct | 66187002 | Steatorrhea | ||
http://snomed.info/sct | 66251001 | Protein conformation | ||
http://snomed.info/sct | 66262001 | Hereditary elliptocytosis due to beta spectrin-ankyrin interaction | ||
http://snomed.info/sct | 66309005 | Antibody-mediated anemia | ||
http://snomed.info/sct | 66552009 | No tissue received | ||
http://snomed.info/sct | 66627000 | Chylous urine | ||
http://snomed.info/sct | 66659007 | Normal variation in position | ||
http://snomed.info/sct | 66790001 | Bacterial growth contamination | ||
http://snomed.info/sct | 66806007 | Sound-induced EEG abnormality | ||
http://snomed.info/sct | 66812002 | Flattened T wave | ||
http://snomed.info/sct | 66876008 | Lambda light chain disease | ||
http://snomed.info/sct | 66887000 | Late syphilis, latent (+ sero., - C.S.F. 2 years after) | ||
http://snomed.info/sct | 66931009 | Hypercalcemia | ||
http://snomed.info/sct | 67023009 | Lymphocytosis | ||
http://snomed.info/sct | 67093004 | Megaloblastic erythropoiesis | ||
http://snomed.info/sct | 67125004 | Latent syphilis (+ sero.) | ||
http://snomed.info/sct | 67132008 | Hypoxic nephrosis | ||
http://snomed.info/sct | 67135005 | Tissue removed at necropsy | ||
http://snomed.info/sct | 67302005 | V1 stage | ||
http://snomed.info/sct | 67544000 | Local untoward skin test reaction | ||
http://snomed.info/sct | 67708007 | Necrospermia | ||
http://snomed.info/sct | 67736002 | Specimen poorly fixed | ||
http://snomed.info/sct | 68036007 | Carbohydrate conformation | ||
http://snomed.info/sct | 68128000 | Urticarial skin test reaction | ||
http://snomed.info/sct | 68256003 | Increased glucose level | ||
http://snomed.info/sct | 68318002 | Decreased platelet destruction | ||
http://snomed.info/sct | 68349007 | DNA damage | ||
http://snomed.info/sct | 68361004 | Late anemia due to isoimmunization | ||
http://snomed.info/sct | 68600005 | Hemoglobinuria | ||
http://snomed.info/sct | 68700003 | Megaloblastic anemia due to error of cobalamin metabolism | ||
http://snomed.info/sct | 68870007 | Congenital dyserythropoietic anemia, type II | ||
http://snomed.info/sct | 68913001 | Alpha thalassaemia syndrome | ||
http://snomed.info/sct | 68979007 | Heavy chain disease | ||
http://snomed.info/sct | 69075005 | Aplastic crisis | ||
http://snomed.info/sct | 69216008 | Hb Lepore thalassemia | ||
http://snomed.info/sct | 69318006 | Shortened ST interval | ||
http://snomed.info/sct | 69329005 | Toxic uninodular goiter with thyrotoxic crisis | ||
http://snomed.info/sct | 69604007 | Abnormal amino acid sequence | ||
http://snomed.info/sct | 69868005 | Genetic operator region | ||
http://snomed.info/sct | 69981004 | Hereditary spherocytosis due to beta spectrin defect | ||
http://snomed.info/sct | 70003006 | Gram-positive cocci in clusters | ||
http://snomed.info/sct | 70804004 | Molecular stability | ||
http://snomed.info/sct | 70918005 | Myeloid hyperplasia of bone marrow | ||
http://snomed.info/sct | 70929009 | Bacterial colony elevation, umbonate | ||
http://snomed.info/sct | 70964000 | Postparturient hemoglobinuria | ||
http://snomed.info/sct | 71269007 | Normal hemostatic function | ||
http://snomed.info/sct | 71436005 | Lazy leukocyte syndrome | ||
http://snomed.info/sct | 71610005 | Neutrophilic leukemoid reaction | ||
http://snomed.info/sct | 71628007 | Abnormal presence of albumin | ||
http://snomed.info/sct | 71692003 | Leukoerythroblastotic reaction | ||
http://snomed.info/sct | 71716005 | Erythrocytosis due to renal cyst | ||
http://snomed.info/sct | 71785001 | Water intoxication syndrome | ||
http://snomed.info/sct | 71832003 | Autoimmune hemolytic anemia caused by immunoglobulin M | ||
http://snomed.info/sct | 71938000 | Hypercalciuria | ||
http://snomed.info/sct | 71988008 | Aase syndrome | ||
http://snomed.info/sct | 72500007 | Normal variation in consistency | ||
http://snomed.info/sct | 72632003 | L2 stage | ||
http://snomed.info/sct | 72633008 | Base sequence | ||
http://snomed.info/sct | 72644000 | Gene re-arrangement, alpha chain, T cell antigen receptor | ||
http://snomed.info/sct | 72724002 | Morphologic finding | ||
http://snomed.info/sct | 72959009 | Molecular inactivation | ||
http://snomed.info/sct | 73014008 | Pyogenic proteinuria | ||
http://snomed.info/sct | 73073009 | Hereditary elliptocytosis due to beta spectrin defect in self-association | ||
http://snomed.info/sct | 73162004 | Posttransfusion purpura | ||
http://snomed.info/sct | 73190000 | Epsilon gamma delta beta^0^ thalassemia | ||
http://snomed.info/sct | 73238002 | Shrinkage | ||
http://snomed.info/sct | 73255003 | Megaloblastoid erythropoiesis | ||
http://snomed.info/sct | 73397007 | Heparin-induced thrombocytopenia | ||
http://snomed.info/sct | 73630001 | Prerenal proteinuria | ||
http://snomed.info/sct | 73784008 | Tissue surgically removed | ||
http://snomed.info/sct | 73804003 | Homology region | ||
http://snomed.info/sct | 73869005 | Toxic uninodular goiter | ||
http://snomed.info/sct | 73883007 | Emulsion proteinuria | ||
http://snomed.info/sct | 73999000 | Posterior infarction by EKG | ||
http://snomed.info/sct | 74003001 | Hyponatremia with normal extracellular fluid volume | ||
http://snomed.info/sct | 74139005 | L1 stage | ||
http://snomed.info/sct | 74185008 | Hyponatremia with extracellular fluid depletion | ||
http://snomed.info/sct | 74256009 | DNA replication | ||
http://snomed.info/sct | 74354009 | Nucleic acid sequence homology | ||
http://snomed.info/sct | 74428002 | Genetic transfection | ||
http://snomed.info/sct | 74576004 | Acquired thrombocytopenia | ||
http://snomed.info/sct | 74599000 | No microscopic confirmation - clinically malignant tumor (cancer) | ||
http://snomed.info/sct | 74703006 | Pyruvate kinase deficiency anemia | ||
http://snomed.info/sct | 74789008 | Coombs positive hemolytic anemia | ||
http://snomed.info/sct | 74836001 | Secretor gene present (Se) | ||
http://snomed.info/sct | 75063005 | Hemoglobinopathy with erythrocytosis | ||
http://snomed.info/sct | 75083006 | Increased osmotic fragility | ||
http://snomed.info/sct | 75117001 | Bacterial colony shape | ||
http://snomed.info/sct | 75331009 | Evans syndrome | ||
http://snomed.info/sct | 75443009 | Hereditary elliptocytosis due to abnormal protein 4.1 | ||
http://snomed.info/sct | 75451007 | Thalassemia major | ||
http://snomed.info/sct | 75492003 | Bacterial colony consistency, membranous | ||
http://snomed.info/sct | 75843002 | Bacterial colony density, opaque | ||
http://snomed.info/sct | 75900009 | Bacterial colony density, translucent | ||
http://snomed.info/sct | 75944007 | Decreased platelet life span | ||
http://snomed.info/sct | 76291004 | Fine granular consistency | ||
http://snomed.info/sct | 76336008 | Delta beta zero thalassemia | ||
http://snomed.info/sct | 76366001 | Hemolytic anemia caused by Bartonella | ||
http://snomed.info/sct | 76388001 | ST segment elevation | ||
http://snomed.info/sct | 76397002 | Normal variation in distribution | ||
http://snomed.info/sct | 76602008 | Superhelicity | ||
http://snomed.info/sct | 76612001 | Hypercoagulability state | ||
http://snomed.info/sct | 76762001 | Eosinophilic myopathy | ||
http://snomed.info/sct | 76873001 | Polycythemia due to maternal-fetal transfusion | ||
http://snomed.info/sct | 76908005 | Lactose factor | ||
http://snomed.info/sct | 77084001 | Immunologic aplastic anemia | ||
http://snomed.info/sct | 77092005 | Bacterial colony surface, rough | ||
http://snomed.info/sct | 77250007 | Essential proteinuria | ||
http://snomed.info/sct | 77289001 | Insufficient tissue for diagnosis | ||
http://snomed.info/sct | 77324006 | Bacterial colony shape, spindle | ||
http://snomed.info/sct | 77413008 | Severe hereditary spherocytosis due to spectrin deficiency | ||
http://snomed.info/sct | 77483002 | Febrile urine | ||
http://snomed.info/sct | 77566008 | Right atrial hypertrophy by EKG | ||
http://snomed.info/sct | 77663007 | Hemolytic anemia due to malaria | ||
http://snomed.info/sct | 77867006 | Shortened QT interval | ||
http://snomed.info/sct | 78129009 | Thrombotic thrombocytopenic purpura | ||
http://snomed.info/sct | 78209002 | Hemolytic uremic syndrome, adult type | ||
http://snomed.info/sct | 78345002 | Thrombocytopenia due to diminished platelet production | ||
http://snomed.info/sct | 78378009 | Isoimmune neutropenia | ||
http://snomed.info/sct | 78473004 | Gene re-arrangement, beta chain, T cell antigen receptor | ||
http://snomed.info/sct | 78544004 | Chronic hypertensive uremia | ||
http://snomed.info/sct | 78578005 | Erythrocytosis due to pulmonary disease | ||
http://snomed.info/sct | 78867009 | Decreased erythrocyte life span | ||
http://snomed.info/sct | 78908001 | HNSHA due to decreased adenosine deaminase activity | ||
http://snomed.info/sct | 79248008 | Blood group A>1<B | ||
http://snomed.info/sct | 79268002 | POEMS syndrome | ||
http://snomed.info/sct | 79336007 | Familial eosinophilia | ||
http://snomed.info/sct | 79592006 | Beta plus thalassemia | ||
http://snomed.info/sct | 79667004 | Abnormal macromolecular sequence | ||
http://snomed.info/sct | 80119007 | Pericarditis secondary to uremia | ||
http://snomed.info/sct | 80126007 | Plummer-Vinson syndrome | ||
http://snomed.info/sct | 80255009 | Maternal transfer neutropenia | ||
http://snomed.info/sct | 80369006 | Chronic neutrophilia | ||
http://snomed.info/sct | 80511004 | Erythrocytosis due to endocrine disorder (disorder) | ||
http://snomed.info/sct | 80676005 | Bacterial colony hemolysis, alpha | ||
http://snomed.info/sct | 80875006 | Achlorhydric anemia | ||
http://snomed.info/sct | 80963002 | G-6-PD class V variant anemia | ||
http://snomed.info/sct | 81479001 | Macromolecular cleavage | ||
http://snomed.info/sct | 81571000 | Reaction of degeneration by electromyogram | ||
http://snomed.info/sct | 81647003 | Increased serum protein level | ||
http://snomed.info/sct | 81711008 | Drug-induced hemolytic anemia | ||
http://snomed.info/sct | 81835007 | Blood group antigen c^v^ | ||
http://snomed.info/sct | 81919004 | Hybridization | ||
http://snomed.info/sct | 82003006 | G-6-PD class IV variant anemia | ||
http://snomed.info/sct | 82190001 | Thrombocytopenia due to defective platelet production | ||
http://snomed.info/sct | 82275008 | Allergic granulomatosis angiitis | ||
http://snomed.info/sct | 82281000 | Atrial hypertrophy by EKG | ||
http://snomed.info/sct | 82283002 | Genetic enhancer element | ||
http://snomed.info/sct | 82663009 | Osteopathia striata | ||
http://snomed.info/sct | 82835005 | Neonatal thrombocytopenia | ||
http://snomed.info/sct | 82895008 | Megaloblastic anemia due to disease of small intestine | ||
http://snomed.info/sct | 83370008 | Ventricular hypertrophy by EKG | ||
http://snomed.info/sct | 83442007 | Systemic untoward skin test reaction | ||
http://snomed.info/sct | 83464003 | Increased markings | ||
http://snomed.info/sct | 83484004 | Abnormal translucency | ||
http://snomed.info/sct | 83579008 | Mixed gonadal dysgenesis | ||
http://snomed.info/sct | 83850008 | Uremic acidosis | ||
http://snomed.info/sct | 84188003 | Thalassemia syndrome | ||
http://snomed.info/sct | 84324009 | Bacterial colony color | ||
http://snomed.info/sct | 84567002 | Specimen obscured by blood | ||
http://snomed.info/sct | 84625002 | Acute febrile neutrophilic dermatosis | ||
http://snomed.info/sct | 84697003 | Decreased plasma volume | ||
http://snomed.info/sct | 84828003 | Leukopenia | ||
http://snomed.info/sct | 84937002 | Cerebral hyponatremia | ||
http://snomed.info/sct | 85030005 | RNA splicing | ||
http://snomed.info/sct | 85090007 | Dextrocardia/situs inversus finding | ||
http://snomed.info/sct | 85422000 | Alpha plus thalassemia non deletion type (disorder) | ||
http://snomed.info/sct | 85557000 | HPFH deletion type | ||
http://snomed.info/sct | 85559002 | Pelger-Huët anomaly | ||
http://snomed.info/sct | 85589009 | Radial aplasia-thrombocytopenia syndrome | ||
http://snomed.info/sct | 85599004 | Gene template | ||
http://snomed.info/sct | 85607003 | Morphology unknown | ||
http://snomed.info/sct | 85728002 | Morphologic description only | ||
http://snomed.info/sct | 85764001 | Bacterial colony morphology, curled margin | ||
http://snomed.info/sct | 85897006 | Bacterial colony hemolysis, beta | ||
http://snomed.info/sct | 85900004 | Proband | ||
http://snomed.info/sct | 85938000 | Synteny | ||
http://snomed.info/sct | 86069005 | Breslow measurement - depth less than 0.76 mm (finding) | ||
http://snomed.info/sct | 86134005 | Normal position | ||
http://snomed.info/sct | 86140003 | Cosmid | ||
http://snomed.info/sct | 86225009 | Hapten type high affinity hemolytic anemia | ||
http://snomed.info/sct | 86242003 | Alpha plus thalassaemia deletion type | ||
http://snomed.info/sct | 86457007 | Nucleic acid regulatory sequence | ||
http://snomed.info/sct | 86635005 | Kasabach-Merritt syndrome | ||
http://snomed.info/sct | 86715000 | Beta 0 thalassemia | ||
http://snomed.info/sct | 86725005 | Bacterial colony elevation | ||
http://snomed.info/sct | 86734000 | Bacterial colony morphology, erose margin | ||
http://snomed.info/sct | 86859003 | G-6-PD variant enzyme deficiency anemia | ||
http://snomed.info/sct | 86902002 | Dispersion | ||
http://snomed.info/sct | 86986002 | Rh hemolytic disease of the newborn | ||
http://snomed.info/sct | 86991001 | Abnormal consistency | ||
http://snomed.info/sct | 87066005 | Decreased fibrinolysis | ||
http://snomed.info/sct | 87361006 | Left shift of WBC | ||
http://snomed.info/sct | 87469009 | Left atrial hypertrophy by EKG | ||
http://snomed.info/sct | 87522002 | Iron deficiency anemia | ||
http://snomed.info/sct | 87523007 | Increased macromolecular binding | ||
http://snomed.info/sct | 87682005 | Gene re-arrangement, B lymphocyte | ||
http://snomed.info/sct | 87806008 | Megaloblastic anemia due to tropical sprue | ||
http://snomed.info/sct | 87810006 | Megaloblastic anemia due to alcoholism | ||
http://snomed.info/sct | 87865005 | Adventitious proteinuria | ||
http://snomed.info/sct | 87902006 | Thrombocytopenia due to non-immune destruction | ||
http://snomed.info/sct | 87916001 | Bacterial colony consistency, friable | ||
http://snomed.info/sct | 87956004 | Decreased translucency | ||
http://snomed.info/sct | 88313001 | Bacterial colony elevation, umbilicate | ||
http://snomed.info/sct | 88351001 | Hypercalcemia associated with chronic dialysis | ||
http://snomed.info/sct | 88380005 | Acute milk alkali syndrome | ||
http://snomed.info/sct | 88413002 | Cell type not determined | ||
http://snomed.info/sct | 88458008 | Bacterial growth present | ||
http://snomed.info/sct | 88668007 | Decreased molecular dissociation | ||
http://snomed.info/sct | 88772000 | Abnormal axonal conduction | ||
http://snomed.info/sct | 88854002 | Chronic constitutional pure red cell aplasia | ||
http://snomed.info/sct | 88861003 | Decreased heme-heme interaction | ||
http://snomed.info/sct | 88942003 | Blood group A>2<B | ||
http://snomed.info/sct | 89017001 | Gene re-arrangement, B lymphocyte, light chain | ||
http://snomed.info/sct | 89109006 | Blood group antigen D^u^ | ||
http://snomed.info/sct | 89238002 | True proteinuria | ||
http://snomed.info/sct | 89327000 | Increased heme-heme interaction | ||
http://snomed.info/sct | 89454001 | Shwachman syndrome | ||
http://snomed.info/sct | 89459006 | HPFH linked to beta-globulin gene cluster | ||
http://snomed.info/sct | 89470004 | Increased fibrinolysis | ||
http://snomed.info/sct | 89474008 | Negative for metastatic tumor | ||
http://snomed.info/sct | 89551006 | Gene expression | ||
http://snomed.info/sct | 89627008 | Hyponatremia | ||
http://snomed.info/sct | 89647000 | Pyknodysostosis | ||
http://snomed.info/sct | 89655007 | Congenital neutropenia | ||
http://snomed.info/sct | 89743005 | Leuko-araiosis | ||
http://snomed.info/sct | 89744004 | Abnormal carbohydrate sequence | ||
http://snomed.info/sct | 89810003 | ^A^gamma delta beta^0^ thalassemia (disorder) | ||
http://snomed.info/sct | 89936009 | Defective molecular assembly | ||
http://snomed.info/sct | 89962000 | Neonatal thrombocytopenia due to exchange transfusion | ||
http://snomed.info/sct | 89977008 | Increased thickness | ||
http://snomed.info/sct | 90262003 | Normal subcellular morphology | ||
http://snomed.info/sct | 90414007 | Chronic acquired pure red cell aplasia | ||
http://snomed.info/sct | 90469005 | No organoid tissue identified | ||
http://snomed.info/sct | 90501009 | Erythrocytosis due to defective oxygen transport | ||
http://snomed.info/sct | 90578002 | Molecular conformation | ||
http://snomed.info/sct | 90926009 | Bacterial colony surface, smooth | ||
http://snomed.info/sct | 91217009 | Megaloblastic anemia due to pregnancy | ||
http://snomed.info/sct | 91411007 | Autoimmune haemolytic anaemia caused by immunoglobulin A | ||
http://snomed.info/sct | 91504005 | Ineffective thrombopoiesis | ||
http://snomed.info/sct | 91654007 | Bacterial colony consistency | ||
http://snomed.info/sct | 95416007 | Eosinophilia myalgia syndrome | ||
http://snomed.info/sct | 95565000 | Pseudoporphyria | ||
http://snomed.info/sct | 95605009 | HELLP syndrome | ||
http://snomed.info/sct | 95624007 | Neonatal lymphocytopenia | ||
http://snomed.info/sct | 102278006 | Erythrocyte sequestration | ||
http://snomed.info/sct | 102594003 | Abnormal EKG finding | ||
http://snomed.info/sct | 102634007 | Base deficit | ||
http://snomed.info/sct | 102659003 | Normal glucose level | ||
http://snomed.info/sct | 102660008 | Abnormal glucose level | ||
http://snomed.info/sct | 102837003 | Urinary cast, waxy | ||
http://snomed.info/sct | 102838008 | Urinary cast, leukocyte | ||
http://snomed.info/sct | 102840003 | Urinary cast, erythrocyte | ||
http://snomed.info/sct | 102841004 | Urinary cast, fatty | ||
http://snomed.info/sct | 102843001 | Urinary cast, granular | ||
http://snomed.info/sct | 102844007 | Urinary cast, broad | ||
http://snomed.info/sct | 102845008 | Urinary cast, broad waxy | ||
http://snomed.info/sct | 102847000 | Amorphous urinary sediment | ||
http://snomed.info/sct | 102848005 | Fat globules in urine | ||
http://snomed.info/sct | 102851003 | Urinary crystal, ammonium urate | ||
http://snomed.info/sct | 102852005 | Urinary crystal, bilirubin | ||
http://snomed.info/sct | 102853000 | Urinary crystal, calcium carbonate | ||
http://snomed.info/sct | 102854006 | Urinary crystal, calcium oxalate | ||
http://snomed.info/sct | 102855007 | Urinary crystal, calcium phosphate | ||
http://snomed.info/sct | 102856008 | Urinary crystal, calcium sulfate | ||
http://snomed.info/sct | 102857004 | Urinary crystal, cholesterol | ||
http://snomed.info/sct | 102858009 | Urinary crystal, cystine | ||
http://snomed.info/sct | 102859001 | Urinary crystal, hippurate | ||
http://snomed.info/sct | 102860006 | Urinary crystal, leucine | ||
http://snomed.info/sct | 102861005 | Urinary crystal, pyrophosphate | ||
http://snomed.info/sct | 102862003 | Urinary crystal, sulfonamide | ||
http://snomed.info/sct | 102863008 | Urinary crystal, magnesium ammonium phosphate | ||
http://snomed.info/sct | 102864002 | Urinary crystal, tyrosine | ||
http://snomed.info/sct | 102865001 | Uric acid crystalluria | ||
http://snomed.info/sct | 102866000 | Abnormal urine | ||
http://snomed.info/sct | 102958008 | Increased polarization of nerve cell and nerve fiber | ||
http://snomed.info/sct | 102961009 | Normal evoked potential | ||
http://snomed.info/sct | 102962002 | Abnormal evoked potential | ||
http://snomed.info/sct | 102964001 | Normal cerebral evoked potential | ||
http://snomed.info/sct | 102965000 | Abnormal cerebral evoked potential | ||
http://snomed.info/sct | 102970007 | Normal auditory evoked potential | ||
http://snomed.info/sct | 102971006 | Abnormal auditory evoked potential | ||
http://snomed.info/sct | 102973009 | Normal brain stem auditory evoked potential | ||
http://snomed.info/sct | 102974003 | Abnormal brain stem auditory evoked potential | ||
http://snomed.info/sct | 103225004 | Blood group P>2< | ||
http://snomed.info/sct | 103607002 | Acellular smear | ||
http://snomed.info/sct | 103608007 | Specimen less than optimal for diagnosis for lack of clinical information | ||
http://snomed.info/sct | 103609004 | Specimen with abnormal presence of endometrial cells | ||
http://snomed.info/sct | 103610009 | Abnormal presence of endometrial cells in specimen from a menopausal woman | ||
http://snomed.info/sct | 103611008 | Specimen too thick for optimal interpretation | ||
http://snomed.info/sct | 103631007 | Normal quantity of cells | ||
http://snomed.info/sct | 105812000 | Finding related to substance type | ||
http://snomed.info/sct | 106200001 | Hematopoietic system finding | ||
http://snomed.info/sct | 106221001 | Genetic finding | ||
http://snomed.info/sct | 107645002 | Size finding | ||
http://snomed.info/sct | 107646001 | Consistency finding | ||
http://snomed.info/sct | 107648000 | Translucency finding | ||
http://snomed.info/sct | 107652000 | Distribution finding | ||
http://snomed.info/sct | 107674006 | Cytologic finding | ||
http://snomed.info/sct | 109982002 | Alpha heavy chain disease (clinical) | ||
http://snomed.info/sct | 109983007 | Monoclonal gammopathy (clinical) | ||
http://snomed.info/sct | 109984001 | Gamma heavy chain disease (clinical) | ||
http://snomed.info/sct | 109994006 | Essential thrombocythemia (clinical disorder) | ||
http://snomed.info/sct | 110345002 | Normal reticulin | ||
http://snomed.info/sct | 110366005 | Normal estrogen level | ||
http://snomed.info/sct | 110367001 | Increased estrogen level | ||
http://snomed.info/sct | 110368006 | Decreased estrogen level | ||
http://snomed.info/sct | 110370002 | Normal bone marrow iron | ||
http://snomed.info/sct | 110371003 | Abnormal bone marrow iron | ||
http://snomed.info/sct | 110372005 | Increased bone marrow iron | ||
http://snomed.info/sct | 110373000 | Decreased bone marrow iron | ||
http://snomed.info/sct | 110374006 | Absent bone marrow iron | ||
http://snomed.info/sct | 110396000 | No evidence of malignant neoplasm | ||
http://snomed.info/sct | 110440006 | Barr body present, nuclear sex female | ||
http://snomed.info/sct | 110441005 | Barr body absent, nuclear sex male | ||
http://snomed.info/sct | 110442003 | Barr body, more than one present per cell | ||
http://snomed.info/sct | 111001004 | Gammopathy | ||
http://snomed.info/sct | 111407006 | Hemolytic uremic syndrome | ||
http://snomed.info/sct | 111469006 | Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization | ||
http://snomed.info/sct | 111556005 | Diabetic ketoacidosis without coma | ||
http://snomed.info/sct | 111571009 | Congenital atransferrinemia | ||
http://snomed.info/sct | 111572002 | Beta zero thalassemia non deletion type (disorder) | ||
http://snomed.info/sct | 111575000 | Anemia due to membrane defect | ||
http://snomed.info/sct | 111577008 | Anemia due to enzyme deficiency | ||
http://snomed.info/sct | 111579006 | HNSHA due to glutathione synthetase deficiency | ||
http://snomed.info/sct | 111583006 | Leukocytosis | ||
http://snomed.info/sct | 111584000 | Reticular dysgenesis | ||
http://snomed.info/sct | 111585004 | Neutropenia associated with autoimmune disease | ||
http://snomed.info/sct | 111588002 | White clot syndrome | ||
http://snomed.info/sct | 111955002 | Anodal closure clonus | ||
http://snomed.info/sct | 111975006 | Prolonged QT interval | ||
http://snomed.info/sct | 112143006 | ABO group phenotype | ||
http://snomed.info/sct | 112144000 | Blood group A | ||
http://snomed.info/sct | 112149005 | Blood group B | ||
http://snomed.info/sct | 112211004 | Genetic translation | ||
http://snomed.info/sct | 112212006 | Extra chromosomal inheritance | ||
http://snomed.info/sct | 112631006 | Specimen unsatisfactory for diagnosis | ||
http://snomed.info/sct | 113047000 | Bacterial colony shape, rhizoid | ||
http://snomed.info/sct | 115265008 | Urinary crystal, phosphate | ||
http://snomed.info/sct | 115594000 | Urinary crystal, amorphous urate (finding) | ||
http://snomed.info/sct | 115595004 | Urinary crystal, amorphous phosphate | ||
http://snomed.info/sct | 115665000 | Atopic state | ||
http://snomed.info/sct | 115730009 | Hh blood group phenotype | ||
http://snomed.info/sct | 115731008 | Blood group O>h< Bombay | ||
http://snomed.info/sct | 115732001 | Blood group O>h< Bombay Indian type | ||
http://snomed.info/sct | 115734000 | Blood group O>h< Bombay Reunion type | ||
http://snomed.info/sct | 115735004 | Blood group Para-Bombay | ||
http://snomed.info/sct | 115736003 | Blood group A>h< | ||
http://snomed.info/sct | 115737007 | Blood group B>h< | ||
http://snomed.info/sct | 115748000 | Lewis blood group phenotype | ||
http://snomed.info/sct | 115749008 | Le(a-b-) phenotype | ||
http://snomed.info/sct | 115750008 | I blood group phenotype | ||
http://snomed.info/sct | 115751007 | i>cord< phenotype | ||
http://snomed.info/sct | 115752000 | i>adult< phenotype | ||
http://snomed.info/sct | 115753005 | i>1< phenotype | ||
http://snomed.info/sct | 115754004 | i>2< phenotype | ||
http://snomed.info/sct | 115755003 | I phenotype | ||
http://snomed.info/sct | 115756002 | I>int< phenotype | ||
http://snomed.info/sct | 115758001 | Rhesus blood group phenotype | ||
http://snomed.info/sct | 115759009 | Rh>null< phenotype | ||
http://snomed.info/sct | 115760004 | X^o^rX^o^r blood group phenotype | ||
http://snomed.info/sct | 115761000 | Rr^-^ blood group phenotype | ||
http://snomed.info/sct | 115762007 | Rh>mod< blood group phenotype | ||
http://snomed.info/sct | 115763002 | Trans weak D phenotype | ||
http://snomed.info/sct | 115764008 | Inherited weak D phenotype | ||
http://snomed.info/sct | 115794002 | P blood group phenotype | ||
http://snomed.info/sct | 115795001 | P>1< phenotype | ||
http://snomed.info/sct | 115796000 | P>1<^k^ phenotype | ||
http://snomed.info/sct | 115797009 | P>2<^k^ phenotype | ||
http://snomed.info/sct | 115798004 | Landsteiner-Wiener phenotype | ||
http://snomed.info/sct | 115799007 | LW(a-b-) phenotype |
Explanation of the columns that may appear on this page:
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |
IG © 2021+ HL7 International / Public Health. Package hl7.fhir.uv.shc-vaccination#1.0.0 based on FHIR 4.0.1. Generated 2026-02-19
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