SMART Health Cards: Vaccination & Testing Implementation Guide
1.0.0 - STU1 Release International flag

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

ValueSet: Lab result findings (SNOMED CT)

Official URL: http://hl7.org/fhir/uv/shc-vaccination/ValueSet/lab-result-findings Version: 1.0.0
Draft as of 2024-12-04 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

This value set includes SNOMED CT codes for identifying laboratory test results.

References

Logical Definition (CLD)

Generated Narrative: ValueSet lab-result-findings

This value set includes codes based on the following rules:

 

Expansion

Generated Narrative: ValueSet

Expansion based on SNOMED CT International edition 01-Aug 2024

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

CodeSystemDisplay
  183005http://snomed.info/sctAutoimmune pancytopenia
  292003http://snomed.info/sctEEG finding
  398002http://snomed.info/sctLeft axis deviation greater than -90 degrees by EKG
  437009http://snomed.info/sctAbnormal composition of urine
  479003http://snomed.info/sctGraves' disease with pretibial myxedema AND with thyrotoxic crisis
  518002http://snomed.info/sctMultiple aggregation
  816009http://snomed.info/sctGenetic recombination
  827006http://snomed.info/sctLate congenital syphilis, latent (+ sero., - C.S.F., 2 years OR more)
  842009http://snomed.info/sctConsanguinity
  934007http://snomed.info/sctThalassemia intermedia
  991002http://snomed.info/sctWide QRS complex
  1077002http://snomed.info/sctSeptal infarction by EKG
  1107004http://snomed.info/sctEarly latent syphilis, positive serology, negative cerebrospinal fluid, with relapse after treatment (disorder)
  1152001http://snomed.info/sctSkin reaction negative
  1155004http://snomed.info/sctEKG hypertrophy
  1168007http://snomed.info/sctAllotype
  1318006http://snomed.info/sctPost-translational genetic protein processing
  1393001http://snomed.info/sctLenz-Majewski hyperostosis syndrome
  1592005http://snomed.info/sctFailed attempted abortion with uremia
  1663004http://snomed.info/sctG2 stage
  1777007http://snomed.info/sctIncreased molecular dissociation
  2243000http://snomed.info/sctHypercalcemia due to hyperthyroidism
  2308003http://snomed.info/sctSilent alleles
  2351004http://snomed.info/sctGenetic transduction
  2388001http://snomed.info/sctNormal variation in translucency
  2398007http://snomed.info/sctQuinidine toxicity by EKG
  2634004http://snomed.info/sctDecreased blood erythrocyte volume
  2638001http://snomed.info/sctDrug-induced hypercalcaemia
  2657005http://snomed.info/sctOverflow proteinuria
  2663001http://snomed.info/sctPalpatory proteinuria
  2724004http://snomed.info/sctRecruitment
  2740001http://snomed.info/sctGouty proteinuria
  2835000http://snomed.info/sctTraumatic cardiac hemolytic anemia
  2897005http://snomed.info/sctThrombocytopenia due to immune destruction
  2902006http://snomed.info/sctDecreased lymphocyte life span
  2990008http://snomed.info/sctLymphocytic leukemoid reaction
  3067005http://snomed.info/sctBlood group antigen C^u^
  3391005http://snomed.info/sctNegative for tumor cells
  3720003http://snomed.info/sctAbnormal presence of hemoglobin
  3902000http://snomed.info/sctNon dose-related drug-induced neutropenia
  3909009http://snomed.info/sctCoeur en sabot
  3939004http://snomed.info/sctBacterial colony density, transparent
  3947004http://snomed.info/sctHigh oxygen affinity hemoglobin polycythemia
  3978000http://snomed.info/sctHemolytic anemia due to warm antibody
  4575002http://snomed.info/sctAcute hyponatremia
  4854004http://snomed.info/sctAcquired hemolytic anemia
  4939006http://snomed.info/sctHemolytic anemia due to nonlymphoid neoplasm
  4984008http://snomed.info/sctMicrocytic normochromic anemia
  5177007http://snomed.info/sctEKG axis finding
  5277004http://snomed.info/sctUrinary casts
  5300004http://snomed.info/sctHemoglobin Bart's hydrops syndrome
  5315003http://snomed.info/sctAdenosine deaminase superactivity
  5523002http://snomed.info/sctIdiopathic myoglobinuria
  5559008http://snomed.info/sctNormal cellular morphology
  5603006http://snomed.info/sctAutoimmune hemolytic anemia caused by immunoglobulin G (disorder)
  5850000http://snomed.info/sctSuggest repeat smears
  5876000http://snomed.info/sctAcquired pancytopenia
  5967006http://snomed.info/sctA>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis
  5994005http://snomed.info/sctHereditary elliptocytosis due to deficiency of protein 4.1
  6346007http://snomed.info/sctLeukocyte maturation arrest
  6390002http://snomed.info/sctFine dispersion
  6398009http://snomed.info/sctIdiopathic chronic cold agglutinin disease
  6412007http://snomed.info/sctDigitalis toxicity by EKG
  6510002http://snomed.info/sctVX stage
  6631009http://snomed.info/sctThrombocytosis
  6659005http://snomed.info/sctMegaloblastic anemia due to nontropical sprue
  6679002http://snomed.info/sctSpecimen less than optimal for diagnosis
  6800004http://snomed.info/sctBlood group antigen E^u^
  6907002http://snomed.info/sctHemolysin factor
  7085002http://snomed.info/sctHypercalcemia due to sarcoidosis
  7326005http://snomed.info/sctInferior infarction by EKG
  7501002http://snomed.info/sctIncreased lactic acid level
  7599007http://snomed.info/sctGenetic behavior
  7667005http://snomed.info/sctSpecimen shows excessive cytolysis
  7705008http://snomed.info/sctSpecimen inadequate for hormonal evaluation
  7724006http://snomed.info/sctNephritic syndrome
  7766007http://snomed.info/sctCloudy urine
  7923005http://snomed.info/sctMolecular cloning
  8022000http://snomed.info/sctExercise proteinuria
  8116006http://snomed.info/sctPhenotype
  8399009http://snomed.info/sctSkin test reaction conversion
  8857001http://snomed.info/sctHereditary elliptocytosis due to alpha spectrin defect
  8875000http://snomed.info/sctColliquative proteinuria
  9109004http://snomed.info/sctGenetic alleles
  9111008http://snomed.info/sctGlucoglycinuria
  9123002http://snomed.info/sctIncreased turbidity
  9147009http://snomed.info/sctOsteopoikilosis
  9386003http://snomed.info/sctGouty neuritis
  9426002http://snomed.info/sctErythrocytosis due to hydronephrosis
  9437001http://snomed.info/sctAbnormal presence of myoglobin
  9723006http://snomed.info/sctHyperphosphatasemia with bone disease
  9757003http://snomed.info/sctDelayed skin test reaction
  9872007http://snomed.info/sctNormal translucency
  10191004http://snomed.info/sctAnticoagulant effect
  10564005http://snomed.info/sctSevere hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
  10589004http://snomed.info/sctGenetic transcription
  11187001http://snomed.info/sctBacterial colony hemolysis, alpha prime
  11216008http://snomed.info/sctFernandez reaction to lepromin
  11659006http://snomed.info/sctUremic neuropathy
  11781007http://snomed.info/sctAutoimmune hemolytic anemia caused by complement
  11888009http://snomed.info/sctHyperviscosity syndrome
  12178007http://snomed.info/sctNephrogenous proteinuria
  12189000http://snomed.info/sctCoombs negative hemolytic anemia
  12531002http://snomed.info/sctCoarse dispersion
  12534005http://snomed.info/sctUnidentified pathogenic bacteria recovered
  12554006http://snomed.info/sctLaxity
  12645001http://snomed.info/sctGene amplification
  12774002http://snomed.info/sctBacterial colony morphology, entire margin
  12816000http://snomed.info/sctBacterial colony size, large
  12907000http://snomed.info/sctThiamine-responsive megaloblastic anemia
  13172003http://snomed.info/sctChronic idiopathic thrombocytopenic purpura
  13300001http://snomed.info/sctGenetic linkage equilibrium
  13333006http://snomed.info/sctGenetic terminator region
  13465008http://snomed.info/sctBacterial colony elevation, dome shaped
  13500002http://snomed.info/sctElectrocerebral silence
  13644009http://snomed.info/sctHypercholesterolemia
  13703002http://snomed.info/sctNo bacterial antibody increase, paired specimens
  13720003http://snomed.info/sctTriclonal gammopathy
  13930000http://snomed.info/sctAbnormal presence of protein
  14024008http://snomed.info/sctHumoral immunologic aplastic anemia
  14028006http://snomed.info/sctAbnormal thickness
  14087004http://snomed.info/sctHereditary stomatocytosis
  14333004http://snomed.info/sctAlloimmune neonatal neutropenia
  14483005http://snomed.info/sctCoarse granular consistency
  14514008http://snomed.info/sctAnemia due to disturbance of hemoglobin synthesis
  14763005http://snomed.info/sctGouty tophus of pinna
  14915001http://snomed.info/sctGene dosage compensation
  15111002http://snomed.info/sctPelger-Huët cell
  15121005http://snomed.info/sctHereditary elliptocytosis due to glycophorin C deficiency
  15173006http://snomed.info/sctRare organisms
  15212002http://snomed.info/sctAbnormal macromolecular binding
  15232001http://snomed.info/sctIncreased vascular markings of lung
  15268006http://snomed.info/sctAbnormal presence of galactose
  15276008http://snomed.info/sctDrug-induced enzyme deficiency anemia
  15326009http://snomed.info/sctbeta^+^ Thalassemia, normal Hb A>2<, type 2
  15454001http://snomed.info/sctIncreased size
  15466007http://snomed.info/sctErythrocytosis due to cerebellar hemangioma
  15470004http://snomed.info/sctToxic diffuse goiter with acropachy
  15656008http://snomed.info/sctMorphologic diagnosis deferred
  16021003http://snomed.info/sctArtifact due to freezing
  16289009http://snomed.info/sctBacterial growth in animal culture
  16315008http://snomed.info/sctDepolymerization
  16345006http://snomed.info/sctBlood group antigen G^u^
  16360009http://snomed.info/sctDelta-beta thalassemia
  16427007http://snomed.info/sctDelta thalassaemia
  16601003http://snomed.info/sctBacterial colony consistency, viscous
  16618004http://snomed.info/sctPolyclonal gammopathy
  16964007http://snomed.info/sctHereditary persistence of fetal hemoglobin thalassemia
  17221002http://snomed.info/sctBacterial colony elevation, flat
  17235000http://snomed.info/sctSpherocytosis
  17342003http://snomed.info/sctHereditary pure erythrocytosis
  17456000http://snomed.info/sctBreslow measurement - depth from 0.76 to 1.75 mm (finding)
  17523003http://snomed.info/sctGenetic mosaic
  17928001http://snomed.info/sctLight-chain proteinuria
  18250007http://snomed.info/sctDecrease in circumference
  18259008http://snomed.info/sctEEG abnormality without seizure
  18273004http://snomed.info/sctUnstable hemoglobin disease
  18323000http://snomed.info/sctInnocent bystander type hemolytic anemia
  18565007http://snomed.info/sctRedistribution
  19281006http://snomed.info/sctBacterial colony size
  19307009http://snomed.info/sctDrug-induced thrombocytopenic purpura
  19442009http://snomed.info/sctHeterozygous thalassemia
  19482002http://snomed.info/sctRegulatory sequence
  19539001http://snomed.info/sctBacterial colony density
  19588001http://snomed.info/sctErythrocytosis due to tissue hypoxemia
  19636003http://snomed.info/sctMonocytosis
  19730000http://snomed.info/sctAbnormally hard consistency
  19998002http://snomed.info/sctMegakaryocytic maturation arrest
  20329001http://snomed.info/sctLow ventricular voltage by EKG
  21412009http://snomed.info/sctX chromosome-linked pyridoxine refractory sideroblastic anemia
  21845002http://snomed.info/sctGranular consistency
  22061001http://snomed.info/sctHomozygote
  22098000http://snomed.info/sctChronic idiopathic hemolytic anemia
  22310002http://snomed.info/sctChronic idiopathic monocytosis
  22794007http://snomed.info/sctHematogenous proteinuria
  22933009http://snomed.info/sctG-6-PD class I variant anemia
  22986007http://snomed.info/sctTranscriptional RNA splicing
  23132008http://snomed.info/sctAL amyloidosis
  23205009http://snomed.info/sctTransient neonatal thrombocytopenia
  23371004http://snomed.info/sctEpsilon gamma delta beta thalassemia
  23506009http://snomed.info/sctNormal flora
  23624004http://snomed.info/sctBacterial colony surface, creamy
  23875004http://snomed.info/sctNo pathologic diagnosis
  23891001http://snomed.info/sctFebrile proteinuria
  24052000http://snomed.info/sctHypercalcemia due to immobilization
  24122006http://snomed.info/sctInequality in circumference
  24129002http://snomed.info/sctFasciitis with eosinophilia syndrome
  24159007http://snomed.info/sctPersistent lymphocytosis
  24390000http://snomed.info/sctIncreased urobilinogen level
  24403008http://snomed.info/sctP-null phenotype
  24463005http://snomed.info/sctAsthenozoospermia
  24480009http://snomed.info/sctAbnormal nerve conduction
  24595009http://snomed.info/sctPrimary gout
  24620004http://snomed.info/sctHemolytic anemia due to babesiosis
  24652004http://snomed.info/sctDecreased markings
  24661004http://snomed.info/sctG-6-PD class III variant anemia
  24752008http://snomed.info/sctInfantile cortical hyperostosis
  24829000http://snomed.info/sctEosinophilic ulcerative colitis
  24942001http://snomed.info/sctUrobilinogenuria
  24974008http://snomed.info/sctMyelokathexis
  24975009http://snomed.info/sctMild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
  25050002http://snomed.info/sctAlpha heavy chain disease, respiratory form
  25132006http://snomed.info/sctBlood group N>2<
  25194005http://snomed.info/sctAbnormal nucleotide base sequence
  25251008http://snomed.info/sctHNSHA due to gamma glutamyl cysteine synthetase deficiency
  25266006http://snomed.info/sctHereditary spherocytosis due to spectrin deficiency
  25363001http://snomed.info/sctGenetic non disjunction
  25384006http://snomed.info/sctBlood group S>2<
  25443007http://snomed.info/sctX chromosome-linked pyridoxine responsive sideroblastic anemia
  25488008http://snomed.info/sctLeft ventricular hypertrophy by EKG
  25502009http://snomed.info/sctEpisodic lymphocytopenia
  25601009http://snomed.info/sctErythrocytosis due to autotransfusion
  25778006http://snomed.info/sctBacterial colony consistency, butyrous
  25881005http://snomed.info/sctHigh altitude polycythemia
  25900007http://snomed.info/sctGene re-arrangement, B lymphocyte, heavy chain
  26141007http://snomed.info/sctST segment depression
  26151008http://snomed.info/sctGraves' disease with acropachy AND with thyrotoxic crisis
  26165005http://snomed.info/sctIncreased bilirubin level
  26298008http://snomed.info/sctDiabetic coma with ketoacidosis
  26389007http://snomed.info/sctToxic multinodular goiter
  26409005http://snomed.info/sctCongenital dyserythropoietic anemia, type III
  26489008http://snomed.info/sctBacterial colony surface appearance
  26576000http://snomed.info/sctPositive skin test reaction
  26608005http://snomed.info/sctCarbohydrate sequence
  26682008http://snomed.info/sctHomozygous beta thalassemia
  26875006http://snomed.info/sctBacterial colony elevation, convex
  26944003http://snomed.info/sctAcute megaloblastic anemia due to dialysis
  27080008http://snomed.info/sctBeta zero thalassemia deletion type
  27277001http://snomed.info/sctGouty tophus of heart
  27396000http://snomed.info/sctCathodal opening clonus
  27649004http://snomed.info/sctLeft ventricular S-T changes
  27798002http://snomed.info/sctMegaloblastic anemia due to impaired absorption of folate
  27837003http://snomed.info/sctPyle metaphyseal dysplasia
  27863008http://snomed.info/sctNo organisms seen
  27868004http://snomed.info/sctChronic steatorrhea
  28147001http://snomed.info/sctHaemolytic anaemia caused by Clostridium welchii
  28166001http://snomed.info/sctMolecular degradation
  28319009http://snomed.info/sctErythrocytosis due to cardiovascular disease
  28328005http://snomed.info/sctRadiologic markings
  28428009http://snomed.info/sctVisceral gout
  28630001http://snomed.info/sctShortened QRS complex
  28798000http://snomed.info/sctSubstance not assigned to a scientific category
  28820008http://snomed.info/sctAmino acid sequence
  28965003http://snomed.info/sctDeficiency of DNA repair
  28975000http://snomed.info/sctConstitutional aplastic anemia
  29082008http://snomed.info/sctNormal stimulus response of nerve cell and nerve fiber
  29120000http://snomed.info/sctEosinophilic colitis
  29177004http://snomed.info/sctAnemia due to pentose phosphate pathway defect
  29230002http://snomed.info/sctBacterial growth in artificial medium
  29286002http://snomed.info/sctAbnormal nucleic acid sequence
  29489007http://snomed.info/sctEKG axis perpendicular to frontal plane
  29549004http://snomed.info/sctRRNA operon
  29738008http://snomed.info/sctProteinuria
  29746009http://snomed.info/sctNormal distribution
  29789008http://snomed.info/sctMonocytic leukemoid reaction
  30182008http://snomed.info/sctThrombocytopenia due to extracorporeal circulation (disorder)
  30257002http://snomed.info/sctAbnormal fibrinolysis
  30271005http://snomed.info/sctBacterial colony surface, granular
  30389008http://snomed.info/sctNormal tissue
  30453001http://snomed.info/sctAbnormal molecular cross-linking
  30575002http://snomed.info/sctFanconi pancytopenia syndrome
  30981000http://snomed.info/sctSecondary eosinophilia
  30985009http://snomed.info/sctToxic nodular goiter with thyrotoxic storm
  31091003http://snomed.info/sctSister chromatid exchange
  31137003http://snomed.info/sctEarly latent syphilis, positive serology, negative cerebrospinal fluid, less than 2 years after infection (disorder)
  31153000http://snomed.info/sctBacterial colony shape, filamentous
  31563000http://snomed.info/sctAsymptomatic bacteriuria in pregnancy
  31649001http://snomed.info/sctAbnormal presence of glucose
  31991001http://snomed.info/sctLeukocytic phagocytosis
  32092008http://snomed.info/sctToxic neutropenia
  32475006http://snomed.info/sctF>2< generation
  32482005http://snomed.info/sctOrthostatic proteinuria
  32648007http://snomed.info/sctMild hereditary spherocytosis due to spectrin deficiency
  32775005http://snomed.info/sctIndeterminate axis by EKG
  32855007http://snomed.info/sctHPFH unlinked to beta-globulin gene cluster
  32858009http://snomed.info/sctHemolytic disease of fetus OR newborn due to ABO immunization
  32984002http://snomed.info/sctNeonatal polycythemia
  33002009http://snomed.info/sctMacromolecular defective synthesis
  33033006http://snomed.info/sctMarch myoglobinuria
  33054004http://snomed.info/sctPolymerization
  33183004http://snomed.info/sctPost infectious thrombocytopenic purpura
  33419001http://snomed.info/sctLX stage
  33491002http://snomed.info/sctAutoimmune hemolytic anemia caused by IgA plus complement
  33513003http://snomed.info/sctFamilial apolipoprotein C-II deficiency
  33779007http://snomed.info/sctBacterial antibody present
  33905008http://snomed.info/sctHereditary spherocytosis due to deficiency of protein 4.2
  34165000http://snomed.info/sctGestational proteinuria
  34194007http://snomed.info/sctHNSHA due to pyrimidine-5'-nucleotidase deficiency
  34216002http://snomed.info/sctProposita
  34225008http://snomed.info/sctIdiopathic hypercalcemia of infancy
  34247008http://snomed.info/sctAnemia due to mechanical damage
  34327003http://snomed.info/sctParturient hemorrhage associated with hyperfibrinolysis
  34349009http://snomed.info/sctFamilial type 5 hyperlipoproteinemia
  34395002http://snomed.info/sctThrombocytopenia due to hypothermia
  34397005http://snomed.info/sctErythrocytosis due to uterine myoma
  34528009http://snomed.info/sctFamilial hypertriglyceridemia
  34643004http://snomed.info/sctDiaphyseal dysplasia
  34782005http://snomed.info/sctChromosomal inheritance
  34850003http://snomed.info/sctBlood group antigen Fy^x^
  34852006http://snomed.info/sctG-6-PD class II variant anemia
  34875004http://snomed.info/sctBacterial colony elevation, raised
  34898007http://snomed.info/sctBacterial colony morphology
  34925000http://snomed.info/sctMegaloblastic anemia due to inborn errors of metabolism
  34993002http://snomed.info/sctMixed proteinuria
  35010007http://snomed.info/sctCathodal closure clonus
  35147005http://snomed.info/sctGenetic crossing over
  35357002http://snomed.info/sctBacterial colony morphology, margin
  35508004http://snomed.info/sctEmpty delta sign
  35703006http://snomed.info/sctTransient paroxysmal cold hemoglobinuria
  35727008http://snomed.info/sctCardiac proteinuria
  35778001http://snomed.info/sctMegaloblastic anemia due to error of folate metabolism
  35868009http://snomed.info/sctCarcinoid syndrome
  36070007http://snomed.info/sctWiskott-Aldrich syndrome
  36222008http://snomed.info/sctCarcinoid heart disease
  36241006http://snomed.info/sctNon-toxic multinodular goiter
  36350006http://snomed.info/sctAbnormally soft consistency
  36351005http://snomed.info/sctAntithrombin III deficiency
  36467003http://snomed.info/sctAlpha plus thalassemia
  36472007http://snomed.info/sctHemoglobin S-F disease
  36506006http://snomed.info/sctNormal thickness
  36568005http://snomed.info/sctHemolytic uremic syndrome of childhood
  36580002http://snomed.info/sctBacterial colony morphology, lobate margin
  36597008http://snomed.info/sctMolecular dissociation
  36601008http://snomed.info/sctCraniometaphyseal dysplasia
  36815008http://snomed.info/sctAcetonuria
  36874002http://snomed.info/sctStress polycythemia
  36898009http://snomed.info/sctFriability
  36919001http://snomed.info/sctAnemia caused by lead
  37097005http://snomed.info/sctErythroblastosis
  37253000http://snomed.info/sctDecreased osmotic fragility
  37398008http://snomed.info/sctDiabetic urine
  37447003http://snomed.info/sctSubstance type not applicable
  37492005http://snomed.info/sctSex-linked thrombocytopenia
  37558005http://snomed.info/sctAbnormal saltatory conduction
  37774003http://snomed.info/sctBacterial colony hemolysis
  37794007http://snomed.info/sctRetraction
  37819008http://snomed.info/sctGenetic sequence homology
  38064006http://snomed.info/sctReactive monocytosis
  38194003http://snomed.info/sctBlood group antigen e^i^
  38531000http://snomed.info/sctDiminished LV forces by EKG
  38638004http://snomed.info/sctIncreased translucency
  38689004http://snomed.info/sctHemolytic anemia due to infection
  38697006http://snomed.info/sctPolycythemia due to donor twin transfusion
  38789009http://snomed.info/sctGenetic dosage effect
  38911009http://snomed.info/sctHereditary hemolytic anemia
  38970002http://snomed.info/sctDoan-Wright syndrome
  39090004http://snomed.info/sctBacterial colony size, small
  39112005http://snomed.info/sctGlutathione synthase deficiency with 5-oxoprolinuria
  39321000http://snomed.info/sctShadow
  39586009http://snomed.info/sctHPFH A gamma beta^+^ thalassemia
  39696006http://snomed.info/sctBacterial colony shape, irregular
  39732003http://snomed.info/sctLeft axis deviation
  39751009http://snomed.info/sctGenetic position effect
  39841003http://snomed.info/sctNormal consistency
  40108008http://snomed.info/sctThalassemia
  40223008http://snomed.info/sctV0 stage
  40233000http://snomed.info/sctNephrotic-nephritic syndrome
  40241000http://snomed.info/sctDenaturation
  40387008http://snomed.info/sctPolyagglutinable erythrocyte syndrome
  40434009http://snomed.info/sctDyspeptic urine
  40679002http://snomed.info/sctErythrocytosis due to alveolar hypoventilation
  40976007http://snomed.info/sctGenetic linkage disequilibrium
  41350008http://snomed.info/sctDecreased granulocyte life span
  41387000http://snomed.info/sctHNSHA due to phosphofructokinase deficiency
  41405005http://snomed.info/sctMuscle fibrillation
  41482005http://snomed.info/sctMolecular sequence data
  41614006http://snomed.info/sctHypoplastic anemia
  41716002http://snomed.info/sctLight-induced EEG abnormality
  41814009http://snomed.info/sctNeutropenia with dysgranulopoiesis
  41835006http://snomed.info/sctReaction of denervation by electromyogram
  41934009http://snomed.info/sctAnalysis for substance type not performed
  42484009http://snomed.info/sctHNSHA due to hexokinase deficiency
  42601008http://snomed.info/sctCongenital hemolytic anemia
  42616006http://snomed.info/sctErythrocytosis due to hepatoma
  42669007http://snomed.info/sctHyponatremia with excess extracellular fluid volume
  42827006http://snomed.info/sctGlobular proteinuria
  42844005http://snomed.info/sctBacterial colony morphology, filamentous margin
  42852008http://snomed.info/sctInfectious lymphocytosis
  42959003http://snomed.info/sctFlare reaction
  43193009http://snomed.info/sctGouty iritis
  43245005http://snomed.info/sctGene re-arrangement
  43258006http://snomed.info/sctMilk alkali syndrome
  43355006http://snomed.info/sctEosinopenia
  43376001http://snomed.info/sctMultiple alleles
  43400009http://snomed.info/sctEEG abnormality with seizure
  43468004http://snomed.info/sctFilling defect
  43515008http://snomed.info/sctSpecimen not representative of anatomic site
  43630006http://snomed.info/sctAnterolateral infarction by EKG
  43707008http://snomed.info/sctAnemia caused by heat (disorder)
  43771008http://snomed.info/sctMorphology not applicable
  43820004http://snomed.info/sctPostrenal proteinuria
  43858000http://snomed.info/sctSecondary aplastic anemia
  43918003http://snomed.info/sctErythrocytosis due to renal tumor
  43996000http://snomed.info/sctNucleic acid conformation
  44206008http://snomed.info/sctHapten type low affinity hemolytic anemia
  44288006http://snomed.info/sctAnemia due to extrinsic red cell abnormality
  44325009http://snomed.info/sctDiminished RV forces by EKG
  44371002http://snomed.info/sctMixed polyclonal cryoimmunoglobulinemia
  44456000http://snomed.info/sctInappropriate secondary erythrocytosis
  44641000http://snomed.info/sctHNSHA due to triosephosphate isomerase deficiency
  44649003http://snomed.info/sctL0 stage
  44666001http://snomed.info/sctMicrocytic hypochromic anemia
  44697002http://snomed.info/sctMelorheostosis
  44724006http://snomed.info/sctAbnormal distribution
  44730006http://snomed.info/sctUremia
  44734002http://snomed.info/sctBacterial colony consistency, brittle
  44815009http://snomed.info/sctBreslow measurement - depth greater than 1.75 mm (finding)
  44832008http://snomed.info/sctIncrease in circumference
  44865000http://snomed.info/sctSecondary polycythemia
  44880006http://snomed.info/sctDecreased macromolecular binding
  44998009http://snomed.info/sctRight ventricular S-T changes
  45113005http://snomed.info/sctSubstance not assigned code in SNOMED
  45154002http://snomed.info/sctGlycosuria
  45212007http://snomed.info/sctF>1< generation
  45280006http://snomed.info/sctBacterial colony surface, glistening
  45427005http://snomed.info/sctHybrid vigor
  45597001http://snomed.info/sctBlood group A>3<B
  45646000http://snomed.info/sctSubacute milk alkali syndrome
  45670001http://snomed.info/sctBacterial colony hemolysis, gamma
  45803000http://snomed.info/sctGenetic promotor region
  45841007http://snomed.info/sctKappa light chain disease
  46049004http://snomed.info/sctReticulocytosis
  46235002http://snomed.info/sctEarly latent congenital syphilis, positive serology, negative spinal fluid (disorder)
  46359005http://snomed.info/sctNeutropenia associated with infectious disease
  46503001http://snomed.info/sctNegative for recurrent tumor
  46760003http://snomed.info/sctEstren-Dameshek anemia
  46784006http://snomed.info/sctCrystalluria
  46785007http://snomed.info/sctFamilial juvenile gout
  47047009http://snomed.info/sctThalassemia with other hemoglobinopathy
  47084006http://snomed.info/sctBeta plus thalassemia normal hemoglobin A>2< type 1 silent (disorder)
  47100003http://snomed.info/sctAnemia of prematurity
  47144000http://snomed.info/sctAcute neutrophilia
  47286004http://snomed.info/sctAggregation
  47318007http://snomed.info/sctDrug-induced neutropenia
  47516005http://snomed.info/sctHereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
  47526003http://snomed.info/sctHNSHA due to NADH diaphorase deficiency
  47665007http://snomed.info/sctRight axis deviation
  47708004http://snomed.info/sctGenetic predisposition
  47709007http://snomed.info/sctHumoral hypercalcemia of malignancy
  47739002http://snomed.info/sctMyelophthisis
  47740000http://snomed.info/sctBacterial colony surface, dull
  47872005http://snomed.info/sctHypoviscosity
  47973001http://snomed.info/sctArtifact
  47986005http://snomed.info/sctGenetic anomaly of leukocyte
  48160003http://snomed.info/sctLordotic proteinuria
  48165008http://snomed.info/sctMyoglobinuria
  48188009http://snomed.info/sctAzoospermia
  48250002http://snomed.info/sctGaisbock's syndrome
  48408000http://snomed.info/sctBacterial colony morphology, undulate margin
  48440001http://snomed.info/sctArticular gout
  48516007http://snomed.info/sctAcute infectious lymphocytosis
  48553001http://snomed.info/sctHemoglobin H disease
  48744006http://snomed.info/sctNormal variation in thickness
  48788004http://snomed.info/sctCyclic thrombocytopenia
  48796009http://snomed.info/sctCongenital nephrotic syndrome
  48813009http://snomed.info/sctLymphocytopenia
  48883003http://snomed.info/sctSpecimen satisfactory for diagnosis
  48983004http://snomed.info/sctX chromosome-linked sideroblastic anemia
  49030004http://snomed.info/sctStrand breaks
  49099001http://snomed.info/sctIncreased uric acid level
  49284006http://snomed.info/sctJuvenile type megaloblastic anemia
  49578007http://snomed.info/sctShortened PR interval
  49621008http://snomed.info/sctGouty urine
  49886003http://snomed.info/sctThrombocytopenia due to blood loss
  50004001http://snomed.info/sctNo substance type identified
  50064003http://snomed.info/sctV2 stage
  50110003http://snomed.info/sctNo endocervical cells present
  50220002http://snomed.info/sctCellular immunologic aplastic anemia
  50253007http://snomed.info/sctSecondary paroxysmal cold hemoglobinuria
  50296002http://snomed.info/sctLipid conformation
  50311009http://snomed.info/sctErythrocyte aggregation
  50327002http://snomed.info/sctChronic hyponatremia
  50334000http://snomed.info/sctGenetic polymorphism
  50551008http://snomed.info/sctRight shift of WBC
  50606000http://snomed.info/sctGenetic selection
  50715003http://snomed.info/sctPure red cell aplasia
  50820005http://snomed.info/sctCytopenia
  50935005http://snomed.info/sctMilky urine
  51028009http://snomed.info/sctAbnormal presence of pentose
  51071000http://snomed.info/sctMicroangiopathic hemolytic anemia
  51183001http://snomed.info/sctUntoward skin test reaction
  51291001http://snomed.info/sctNegative for residual tumor
  51319002http://snomed.info/sctLight chain disease
  51381009http://snomed.info/sctIncreased diameter
  51512005http://snomed.info/sctNucleic acid repetitive sequence
  51624005http://snomed.info/sctDilutional thrombocytopenia
  51798006http://snomed.info/sctDecreased glucose level
  51982005http://snomed.info/sctEmulsification
  52064007http://snomed.info/sctBiclonal gammopathy
  52212006http://snomed.info/sctHNSHA due to glutathione reductase deficiency
  52254009http://snomed.info/sctNephrotic syndrome
  52413004http://snomed.info/sctHNSHA due to glucose phosphate isomerase deficiency
  52691008http://snomed.info/sctNo microscopic confirmation - clinically metastatic tumor (cancer)
  52760008http://snomed.info/sctHypercalcemia due to granulomatous disease
  52816004http://snomed.info/sctGenetic transactivation
  52828007http://snomed.info/sctMacromolecular alteration
  52842004http://snomed.info/sctDecreased turbidity
  52951008http://snomed.info/sctCongenital dyserythropoietic anemia
  52976009http://snomed.info/sctSensitized cell
  53311008http://snomed.info/sctNormal variation in size
  53358000http://snomed.info/sctF factor
  53397008http://snomed.info/sctBiliuria
  53461003http://snomed.info/sctNormal size
  53586009http://snomed.info/sctMacromolecular binding
  53743006http://snomed.info/sctAnemia following fetal blood loss
  54006005http://snomed.info/sctHereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder)
  54079004http://snomed.info/sctAnodal opening clonus
  54082009http://snomed.info/sctBacterial growth in cell culture
  54102005http://snomed.info/sctG1 stage
  54192004http://snomed.info/sctSpecimen obscured by foreign material
  54236009http://snomed.info/sctGenetic replication
  54569005http://snomed.info/sctBernard Soulier syndrome
  54665006http://snomed.info/sctBacterial colony size, medium
  54828006http://snomed.info/sctNucleotide base sequence
  55182004http://snomed.info/sctSurgical margins free of tumor
  55257005http://snomed.info/sctWrong tissue received
  55444004http://snomed.info/sctTransient neonatal neutropenia
  55446002http://snomed.info/sctGenetic mutation
  55662002http://snomed.info/sctEnterogenic proteinuria
  55699002http://snomed.info/sctBacterial colony shape, punctiform
  55759009http://snomed.info/sctIncrease of specific gravity
  55822004http://snomed.info/sctHyperlipidemia
  55907008http://snomed.info/sctAcquired aplastic anemia
  55930002http://snomed.info/sctS-T changes
  55995005http://snomed.info/sctHereditary spherocytosis
  56205004http://snomed.info/sctHPFH nondeletion type
  56260006http://snomed.info/sctProlonged ST segment
  56478004http://snomed.info/sctLeukemoid reaction
  56709009http://snomed.info/sctTarget cell of immunologic reaction
  56879003http://snomed.info/sctGenetic independent segregation
  56918001http://snomed.info/sctDose-related drug-induced neutropenia
  57009009http://snomed.info/sctFunctional proteinuria
  57104001http://snomed.info/sctFinding related to response to skin test
  57160007http://snomed.info/sctFelty's syndrome
  57192008http://snomed.info/sctAcute pure red cell aplasia
  57196006http://snomed.info/sctGene frequency
  57390009http://snomed.info/sctMixed cryoimmunoglobulinemia with monoclonal component
  57557005http://snomed.info/sctChronic milk alkali syndrome
  57652005http://snomed.info/sctBlood group antigen V^u^
  57722009http://snomed.info/sctSensitized red cell
  57777000http://snomed.info/sctToxic nodular goiter
  58136006http://snomed.info/sctNutritional disorder due to calcium-phosphorus imbalance
  58178000http://snomed.info/sctTissue lost in processing
  58460004http://snomed.info/sctBlood group O
  58468006http://snomed.info/sctColicin factor
  58648008http://snomed.info/sctBenign monoclonal gammopathy
  58899004http://snomed.info/sctNo evidence of neoplasm
  59178007http://snomed.info/sctMenkes kinky-hair syndrome
  59462000http://snomed.info/sctDecreased EKG voltage
  59548005http://snomed.info/sctCongenital dyserythropoietic anemia, type I
  59614000http://snomed.info/sctOccult blood in stool
  59635003http://snomed.info/sctNo microscopic confirmation - clinically tumor
  59644002http://snomed.info/sctHNSHA due to phosphoglycerate kinase deficiency
  59763006http://snomed.info/sctHyperphosphatasemia tarda
  59828008http://snomed.info/sctHemolytic crisis
  59931005http://snomed.info/sctInverted T wave
  59957008http://snomed.info/sctNeonatal Graves' disease
  60164003http://snomed.info/sctMegaloblastic anemia due to blind loop syndrome
  60181007http://snomed.info/sctAllelic exclusion
  60216004http://snomed.info/sctToxic diffuse goiter with thyrotoxic crisis
  60268006http://snomed.info/sctToxic diffuse goiter with pretibial myxedema
  60399005http://snomed.info/sctDermatofibrosis lenticularis disseminata
  60504009http://snomed.info/sctMegaloblastic anemia due to congenital deficiency of intrinsic factor
  60628003http://snomed.info/sctMediterranean macrothrombocytopenia
  60805002http://snomed.info/sctHemolytic anemia with emphysema AND cutis laxa
  60815008http://snomed.info/sctGrade not determined
  60844005http://snomed.info/sctGenetic inversion
  61026006http://snomed.info/sctG3 stage
  61037007http://snomed.info/sctColloid goiter
  61070002http://snomed.info/sctErythrophagocytosis
  61135002http://snomed.info/sctResidual proteinuria
  61261009http://snomed.info/sctHemolytic anemia
  61373006http://snomed.info/sctBacteriuria
  61395005http://snomed.info/sctHereditary persistence of fetal hemoglobin G gamma beta plus thalassemia
  61493004http://snomed.info/sctMu heavy chain disease
  61596005http://snomed.info/sctHeterophil-positive mononucleosis syndrome
  61609004http://snomed.info/sctGram-positive cocci in chains
  61668005http://snomed.info/sctGene re-arrangement, gamma chain, T cell antigen receptor
  61721007http://snomed.info/sctCounterclockwise vectorcardiographic loop
  61744005http://snomed.info/sctNeonatal thrombocytopenia due to idiopathic maternal thrombocytopenia
  61777009http://snomed.info/sctHemoglobin C-F disease
  61828008http://snomed.info/sctLysogeny
  62074008http://snomed.info/sctDelta zero thalassemia (disorder)
  62117008http://snomed.info/sctBacterial antibody increase, paired specimens
  62268000http://snomed.info/sctHNSHA due to diphosphoglycerate mutase deficiency
  62278002http://snomed.info/sctToxic multinodular goiter with thyrotoxic crisis
  62403005http://snomed.info/sctGlucose-6-phosphate dehydrogenase deficiency anemia
  62410004http://snomed.info/sctPostpartum fibrinolysis with hemorrhage
  62609001http://snomed.info/sctAutoimmune haemolytic anaemia caused by immunoglobulin G plus complement
  62781006http://snomed.info/sctIncreased platelet destruction
  62803002http://snomed.info/sctFrontometaphyseal dysplasia
  62871001http://snomed.info/sctIdiopathic paroxysmal cold hemoglobinuria
  62938001http://snomed.info/sctNormal strength-duration relationship of nerve cell and nerve fiber
  63038006http://snomed.info/sctSpecimen obscured by inflammation
  63092005http://snomed.info/sctImmediate skin test reaction
  63192007http://snomed.info/sctDecreased uric acid level
  63325007http://snomed.info/sctMolecular aggregation
  63444004http://snomed.info/sctThrombocytopenia due to hypersplenism
  63484008http://snomed.info/sctDrug-induced neutrophilia
  63565007http://snomed.info/sctCongenital anemia
  63583004http://snomed.info/sctSolitary aggregation
  63672004http://snomed.info/sctAbsent skin test reaction
  63693001http://snomed.info/sctGenetic transformation
  63919000http://snomed.info/sctR factor
  64088006http://snomed.info/sctHyperviscosity
  64195000http://snomed.info/sctGenetic variation
  64245008http://snomed.info/sctPropositus
  64249002http://snomed.info/sctAllergic eosinophilia
  64553001http://snomed.info/sctSecretor gene absent (se)
  64668006http://snomed.info/sctSensitized leukocyte
  64781005http://snomed.info/sctBacterial colony shape, circular
  64936001http://snomed.info/sctLöffler's syndrome
  64970000http://snomed.info/sctSubstance type unknown
  65087006http://snomed.info/sctBlood group M>2<
  65113001http://snomed.info/sctDNA repair
  65209002http://snomed.info/sctBasophilia
  65230006http://snomed.info/sctHeterophil-negative mononucleosis syndrome
  65247007http://snomed.info/sctGene re-arrangement, T lymphocyte
  65264005http://snomed.info/sctMacromolecular nicking
  65476007http://snomed.info/sctAbnormal size
  65533007http://snomed.info/sctSensitized platelet
  65623009http://snomed.info/sctImmune neutropenia
  65712000http://snomed.info/sctNo microscopic confirmation - clinically benign tumor
  65783004http://snomed.info/sctConjugative plasmid
  65798002http://snomed.info/sctMolecular cross-linking
  65959000http://snomed.info/sctBeta thalassemia
  66055002http://snomed.info/sctAlpha zero thalassemia
  66115002http://snomed.info/sctMolecular instability
  66187002http://snomed.info/sctSteatorrhea
  66251001http://snomed.info/sctProtein conformation
  66262001http://snomed.info/sctHereditary elliptocytosis due to beta spectrin-ankyrin interaction
  66309005http://snomed.info/sctAntibody-mediated anemia
  66552009http://snomed.info/sctNo tissue received
  66627000http://snomed.info/sctChylous urine
  66659007http://snomed.info/sctNormal variation in position
  66790001http://snomed.info/sctBacterial growth contamination
  66806007http://snomed.info/sctSound-induced EEG abnormality
  66812002http://snomed.info/sctFlattened T wave
  66876008http://snomed.info/sctLambda light chain disease
  66887000http://snomed.info/sctLate syphilis, latent (+ sero., - C.S.F. 2 years after)
  66931009http://snomed.info/sctHypercalcemia
  67023009http://snomed.info/sctLymphocytosis
  67125004http://snomed.info/sctLatent syphilis (+ sero.)
  67132008http://snomed.info/sctHypoxic nephrosis
  67135005http://snomed.info/sctTissue removed at necropsy
  67148009http://snomed.info/sctPodagra
  67302005http://snomed.info/sctV1 stage
  67544000http://snomed.info/sctLocal untoward skin test reaction
  67708007http://snomed.info/sctNecrospermia
  67736002http://snomed.info/sctSpecimen poorly fixed
  68036007http://snomed.info/sctCarbohydrate conformation
  68128000http://snomed.info/sctUrticarial skin test reaction
  68256003http://snomed.info/sctIncreased glucose level
  68318002http://snomed.info/sctDecreased platelet destruction
  68349007http://snomed.info/sctDNA damage
  68361004http://snomed.info/sctLate anemia due to isoimmunization
  68451005http://snomed.info/sctChronic gouty arthritis
  68600005http://snomed.info/sctHemoglobinuria
  68700003http://snomed.info/sctMegaloblastic anemia due to error of cobalamin metabolism
  68870007http://snomed.info/sctCongenital dyserythropoietic anemia, type II
  68913001http://snomed.info/sctAlpha thalassaemia syndrome
  68979007http://snomed.info/sctHeavy chain disease
  69075005http://snomed.info/sctAplastic crisis
  69216008http://snomed.info/sctHb Lepore thalassemia
  69318006http://snomed.info/sctShortened ST interval
  69329005http://snomed.info/sctToxic uninodular goiter with thyrotoxic crisis
  69604007http://snomed.info/sctAbnormal amino acid sequence
  69868005http://snomed.info/sctGenetic operator region
  69981004http://snomed.info/sctHereditary spherocytosis due to beta spectrin defect
  70003006http://snomed.info/sctGram-positive cocci in clusters
  70804004http://snomed.info/sctMolecular stability
  70918005http://snomed.info/sctMyeloid hyperplasia of bone marrow
  70929009http://snomed.info/sctBacterial colony elevation, umbonate
  70964000http://snomed.info/sctPostparturient hemoglobinuria
  71269007http://snomed.info/sctNormal hemostatic function
  71436005http://snomed.info/sctLazy leukocyte syndrome
  71610005http://snomed.info/sctNeutrophilic leukemoid reaction
  71628007http://snomed.info/sctAbnormal presence of albumin
  71692003http://snomed.info/sctLeukoerythroblastotic reaction
  71716005http://snomed.info/sctErythrocytosis due to renal cyst
  71785001http://snomed.info/sctWater intoxication syndrome
  71832003http://snomed.info/sctAutoimmune hemolytic anemia caused by immunoglobulin M
  71988008http://snomed.info/sctAase syndrome
  72500007http://snomed.info/sctNormal variation in consistency
  72632003http://snomed.info/sctL2 stage
  72633008http://snomed.info/sctBase sequence
  72644000http://snomed.info/sctGene re-arrangement, alpha chain, T cell antigen receptor
  72724002http://snomed.info/sctMorphologic finding
  72959009http://snomed.info/sctMolecular inactivation
  73014008http://snomed.info/sctPyogenic proteinuria
  73073009http://snomed.info/sctHereditary elliptocytosis due to beta spectrin defect in self-association
  73162004http://snomed.info/sctPosttransfusion purpura
  73190000http://snomed.info/sctEpsilon gamma delta beta^0^ thalassemia
  73238002http://snomed.info/sctShrinkage
  73255003http://snomed.info/sctMegaloblastoid erythropoiesis
  73397007http://snomed.info/sctHeparin-induced thrombocytopenia
  73630001http://snomed.info/sctPrerenal proteinuria
  73784008http://snomed.info/sctTissue surgically removed
  73804003http://snomed.info/sctHomology region
  73869005http://snomed.info/sctToxic uninodular goiter
  73883007http://snomed.info/sctEmulsion proteinuria
  73999000http://snomed.info/sctPosterior infarction by EKG
  74003001http://snomed.info/sctHyponatremia with normal extracellular fluid volume
  74139005http://snomed.info/sctL1 stage
  74185008http://snomed.info/sctHyponatremia with extracellular fluid depletion
  74256009http://snomed.info/sctDNA replication
  74354009http://snomed.info/sctNucleic acid sequence homology
  74428002http://snomed.info/sctGenetic transfection
  74576004http://snomed.info/sctAcquired thrombocytopenia
  74599000http://snomed.info/sctNo microscopic confirmation - clinically malignant tumor (cancer)
  74703006http://snomed.info/sctPyruvate kinase deficiency anemia
  74789008http://snomed.info/sctCoombs positive hemolytic anemia
  74836001http://snomed.info/sctSecretor gene present (Se)
  75063005http://snomed.info/sctHemoglobinopathy with erythrocytosis
  75083006http://snomed.info/sctIncreased osmotic fragility
  75117001http://snomed.info/sctBacterial colony shape
  75331009http://snomed.info/sctEvans syndrome
  75443009http://snomed.info/sctHereditary elliptocytosis due to abnormal protein 4.1
  75451007http://snomed.info/sctThalassemia major
  75492003http://snomed.info/sctBacterial colony consistency, membranous
  75843002http://snomed.info/sctBacterial colony density, opaque
  75900009http://snomed.info/sctBacterial colony density, translucent
  75944007http://snomed.info/sctDecreased platelet life span
  76291004http://snomed.info/sctFine granular consistency
  76336008http://snomed.info/sctDelta beta zero thalassemia
  76366001http://snomed.info/sctHemolytic anemia caused by Bartonella
  76388001http://snomed.info/sctST segment elevation
  76397002http://snomed.info/sctNormal variation in distribution
  76602008http://snomed.info/sctSuperhelicity
  76612001http://snomed.info/sctHypercoagulability state
  76762001http://snomed.info/sctEosinophilic myopathy
  76873001http://snomed.info/sctPolycythemia due to maternal-fetal transfusion
  76908005http://snomed.info/sctLactose factor
  77084001http://snomed.info/sctImmunologic aplastic anemia
  77092005http://snomed.info/sctBacterial colony surface, rough
  77250007http://snomed.info/sctEssential proteinuria
  77289001http://snomed.info/sctInsufficient tissue for diagnosis
  77324006http://snomed.info/sctBacterial colony shape, spindle
  77413008http://snomed.info/sctSevere hereditary spherocytosis due to spectrin deficiency
  77483002http://snomed.info/sctFebrile urine
  77566008http://snomed.info/sctRight atrial hypertrophy by EKG
  77663007http://snomed.info/sctHemolytic anemia due to malaria
  77867006http://snomed.info/sctShortened QT interval
  78129009http://snomed.info/sctThrombotic thrombocytopenic purpura
  78209002http://snomed.info/sctHemolytic uremic syndrome, adult type
  78345002http://snomed.info/sctThrombocytopenia due to diminished platelet production
  78378009http://snomed.info/sctIsoimmune neutropenia
  78473004http://snomed.info/sctGene re-arrangement, beta chain, T cell antigen receptor
  78544004http://snomed.info/sctChronic hypertensive uremia
  78578005http://snomed.info/sctErythrocytosis due to pulmonary disease
  78867009http://snomed.info/sctDecreased erythrocyte life span
  78908001http://snomed.info/sctHNSHA due to decreased adenosine deaminase activity
  79248008http://snomed.info/sctBlood group A>1<B
  79268002http://snomed.info/sctPOEMS syndrome
  79336007http://snomed.info/sctFamilial eosinophilia
  79592006http://snomed.info/sctBeta plus thalassemia
  79667004http://snomed.info/sctAbnormal macromolecular sequence
  80119007http://snomed.info/sctPericarditis secondary to uremia
  80126007http://snomed.info/sctPlummer-Vinson syndrome
  80255009http://snomed.info/sctMaternal transfer neutropenia
  80369006http://snomed.info/sctChronic neutrophilia
  80511004http://snomed.info/sctErythrocytosis due to endocrine disorder (disorder)
  80676005http://snomed.info/sctBacterial colony hemolysis, alpha
  80875006http://snomed.info/sctAchlorhydric anemia
  80963002http://snomed.info/sctG-6-PD class V variant anemia
  81479001http://snomed.info/sctMacromolecular cleavage
  81571000http://snomed.info/sctReaction of degeneration by electromyogram
  81647003http://snomed.info/sctIncreased serum protein level
  81711008http://snomed.info/sctDrug-induced hemolytic anemia
  81835007http://snomed.info/sctBlood group antigen c^v^
  81919004http://snomed.info/sctHybridization
  82003006http://snomed.info/sctG-6-PD class IV variant anemia
  82190001http://snomed.info/sctThrombocytopenia due to defective platelet production
  82275008http://snomed.info/sctAllergic granulomatosis angiitis
  82281000http://snomed.info/sctAtrial hypertrophy by EKG
  82283002http://snomed.info/sctGenetic enhancer element
  82663009http://snomed.info/sctOsteopathia striata
  82835005http://snomed.info/sctNeonatal thrombocytopenia
  82895008http://snomed.info/sctMegaloblastic anemia due to disease of small intestine
  83370008http://snomed.info/sctVentricular hypertrophy by EKG
  83442007http://snomed.info/sctSystemic untoward skin test reaction
  83464003http://snomed.info/sctIncreased markings
  83484004http://snomed.info/sctAbnormal translucency
  83579008http://snomed.info/sctMixed gonadal dysgenesis
  83850008http://snomed.info/sctUremic acidosis
  84188003http://snomed.info/sctThalassemia syndrome
  84324009http://snomed.info/sctBacterial colony color
  84567002http://snomed.info/sctSpecimen obscured by blood
  84625002http://snomed.info/sctAcute febrile neutrophilic dermatosis
  84697003http://snomed.info/sctDecreased plasma volume
  84828003http://snomed.info/sctLeukopenia
  84937002http://snomed.info/sctCerebral hyponatremia
  85030005http://snomed.info/sctRNA splicing
  85090007http://snomed.info/sctDextrocardia/situs inversus finding
  85422000http://snomed.info/sctAlpha plus thalassemia non deletion type (disorder)
  85557000http://snomed.info/sctHPFH deletion type
  85559002http://snomed.info/sctPelger-Huët anomaly
  85589009http://snomed.info/sctRadial aplasia-thrombocytopenia syndrome
  85599004http://snomed.info/sctGene template
  85607003http://snomed.info/sctMorphology unknown
  85728002http://snomed.info/sctMorphologic description only
  85764001http://snomed.info/sctBacterial colony morphology, curled margin
  85897006http://snomed.info/sctBacterial colony hemolysis, beta
  85900004http://snomed.info/sctProband
  85938000http://snomed.info/sctSynteny
  86069005http://snomed.info/sctBreslow measurement - depth less than 0.76 mm (finding)
  86134005http://snomed.info/sctNormal position
  86140003http://snomed.info/sctCosmid
  86225009http://snomed.info/sctHapten type high affinity hemolytic anemia
  86242003http://snomed.info/sctAlpha plus thalassaemia deletion type
  86457007http://snomed.info/sctNucleic acid regulatory sequence
  86635005http://snomed.info/sctKasabach-Merritt syndrome
  86715000http://snomed.info/sctBeta 0 thalassemia
  86725005http://snomed.info/sctBacterial colony elevation
  86734000http://snomed.info/sctBacterial colony morphology, erose margin
  86859003http://snomed.info/sctG-6-PD variant enzyme deficiency anemia
  86902002http://snomed.info/sctDispersion
  86986002http://snomed.info/sctRh hemolytic disease of the newborn
  86991001http://snomed.info/sctAbnormal consistency
  87066005http://snomed.info/sctDecreased fibrinolysis
  87361006http://snomed.info/sctLeft shift of WBC
  87469009http://snomed.info/sctLeft atrial hypertrophy by EKG
  87522002http://snomed.info/sctIron deficiency anemia
  87523007http://snomed.info/sctIncreased macromolecular binding
  87682005http://snomed.info/sctGene re-arrangement, B lymphocyte
  87806008http://snomed.info/sctMegaloblastic anemia due to tropical sprue
  87810006http://snomed.info/sctMegaloblastic anemia due to alcoholism
  87865005http://snomed.info/sctAdventitious proteinuria
  87902006http://snomed.info/sctThrombocytopenia due to non-immune destruction
  87916001http://snomed.info/sctBacterial colony consistency, friable
  87956004http://snomed.info/sctDecreased translucency
  88313001http://snomed.info/sctBacterial colony elevation, umbilicate
  88351001http://snomed.info/sctHypercalcemia associated with chronic dialysis
  88380005http://snomed.info/sctAcute milk alkali syndrome
  88413002http://snomed.info/sctCell type not determined
  88458008http://snomed.info/sctBacterial growth present
  88668007http://snomed.info/sctDecreased molecular dissociation
  88772000http://snomed.info/sctAbnormal axonal conduction
  88854002http://snomed.info/sctChronic constitutional pure red cell aplasia
  88861003http://snomed.info/sctDecreased heme-heme interaction
  88942003http://snomed.info/sctBlood group A>2<B
  89017001http://snomed.info/sctGene re-arrangement, B lymphocyte, light chain
  89109006http://snomed.info/sctBlood group antigen D^u^
  89238002http://snomed.info/sctTrue proteinuria
  89327000http://snomed.info/sctIncreased heme-heme interaction
  89454001http://snomed.info/sctShwachman syndrome
  89459006http://snomed.info/sctHPFH linked to beta-globulin gene cluster
  89470004http://snomed.info/sctIncreased fibrinolysis
  89474008http://snomed.info/sctNegative for metastatic tumor
  89551006http://snomed.info/sctGene expression
  89627008http://snomed.info/sctHyponatremia
  89647000http://snomed.info/sctPyknodysostosis
  89655007http://snomed.info/sctCongenital neutropenia
  89743005http://snomed.info/sctLeuko-araiosis
  89744004http://snomed.info/sctAbnormal carbohydrate sequence
  89810003http://snomed.info/sct^A^gamma delta beta^0^ thalassemia (disorder)
  89936009http://snomed.info/sctDefective molecular assembly
  89962000http://snomed.info/sctNeonatal thrombocytopenia due to exchange transfusion
  89977008http://snomed.info/sctIncreased thickness
  90262003http://snomed.info/sctNormal subcellular morphology
  90414007http://snomed.info/sctChronic acquired pure red cell aplasia
  90469005http://snomed.info/sctNo organoid tissue identified
  90501009http://snomed.info/sctErythrocytosis due to defective oxygen transport
  90560007http://snomed.info/sctGout
  90578002http://snomed.info/sctMolecular conformation
  90926009http://snomed.info/sctBacterial colony surface, smooth
  91217009http://snomed.info/sctMegaloblastic anemia due to pregnancy
  91411007http://snomed.info/sctAutoimmune haemolytic anaemia caused by immunoglobulin A
  91504005http://snomed.info/sctIneffective thrombopoiesis
  91654007http://snomed.info/sctBacterial colony consistency
  95416007http://snomed.info/sctEosinophilia myalgia syndrome
  95565000http://snomed.info/sctPseudoporphyria
  95605009http://snomed.info/sctHELLP syndrome
  95624007http://snomed.info/sctNeonatal lymphocytopenia
  102278006http://snomed.info/sctErythrocyte sequestration
  102594003http://snomed.info/sctAbnormal EKG finding
  102634007http://snomed.info/sctBase deficit
  102659003http://snomed.info/sctNormal glucose level
  102660008http://snomed.info/sctAbnormal glucose level
  102837003http://snomed.info/sctUrinary cast, waxy
  102838008http://snomed.info/sctUrinary cast, leukocyte
  102840003http://snomed.info/sctUrinary cast, erythrocyte
  102841004http://snomed.info/sctUrinary cast, fatty
  102843001http://snomed.info/sctUrinary cast, granular
  102844007http://snomed.info/sctUrinary cast, broad
  102845008http://snomed.info/sctUrinary cast, broad waxy
  102847000http://snomed.info/sctAmorphous urinary sediment
  102848005http://snomed.info/sctFat globules in urine
  102851003http://snomed.info/sctUrinary crystal, ammonium urate
  102852005http://snomed.info/sctUrinary crystal, bilirubin
  102853000http://snomed.info/sctUrinary crystal, calcium carbonate
  102854006http://snomed.info/sctUrinary crystal, calcium oxalate
  102855007http://snomed.info/sctUrinary crystal, calcium phosphate
  102856008http://snomed.info/sctUrinary crystal, calcium sulfate
  102857004http://snomed.info/sctUrinary crystal, cholesterol
  102858009http://snomed.info/sctUrinary crystal, cystine
  102859001http://snomed.info/sctUrinary crystal, hippurate
  102860006http://snomed.info/sctUrinary crystal, leucine
  102861005http://snomed.info/sctUrinary crystal, pyrophosphate
  102862003http://snomed.info/sctUrinary crystal, sulfonamide
  102863008http://snomed.info/sctUrinary crystal, magnesium ammonium phosphate
  102864002http://snomed.info/sctUrinary crystal, tyrosine
  102865001http://snomed.info/sctUric acid crystalluria
  102866000http://snomed.info/sctAbnormal urine
  102958008http://snomed.info/sctIncreased polarization of nerve cell and nerve fiber
  102961009http://snomed.info/sctNormal evoked potential
  102962002http://snomed.info/sctAbnormal evoked potential
  102964001http://snomed.info/sctNormal cerebral evoked potential
  102965000http://snomed.info/sctAbnormal cerebral evoked potential
  102970007http://snomed.info/sctNormal auditory evoked potential
  102971006http://snomed.info/sctAbnormal auditory evoked potential
  102973009http://snomed.info/sctNormal brain stem auditory evoked potential
  102974003http://snomed.info/sctAbnormal brain stem auditory evoked potential
  103225004http://snomed.info/sctBlood group P>2<
  103607002http://snomed.info/sctAcellular smear
  103608007http://snomed.info/sctSpecimen less than optimal for diagnosis for lack of clinical information
  103609004http://snomed.info/sctSpecimen with abnormal presence of endometrial cells
  103610009http://snomed.info/sctAbnormal presence of endometrial cells in specimen from a menopausal woman
  103611008http://snomed.info/sctSpecimen too thick for optimal interpretation
  103631007http://snomed.info/sctNormal quantity of cells
  105812000http://snomed.info/sctFinding related to substance type
  106200001http://snomed.info/sctHematopoietic system finding
  106221001http://snomed.info/sctGenetic finding
  107645002http://snomed.info/sctSize finding
  107646001http://snomed.info/sctConsistency finding
  107648000http://snomed.info/sctTranslucency finding
  107652000http://snomed.info/sctDistribution finding
  107674006http://snomed.info/sctCytologic finding
  109982002http://snomed.info/sctAlpha heavy chain disease (clinical)
  109983007http://snomed.info/sctMonoclonal gammopathy (clinical)
  109984001http://snomed.info/sctGamma heavy chain disease (clinical)
  109994006http://snomed.info/sctEssential thrombocythemia (clinical disorder)
  110345002http://snomed.info/sctNormal reticulin
  110366005http://snomed.info/sctNormal estrogen level
  110367001http://snomed.info/sctIncreased estrogen level
  110368006http://snomed.info/sctDecreased estrogen level
  110370002http://snomed.info/sctNormal bone marrow iron
  110371003http://snomed.info/sctAbnormal bone marrow iron
  110372005http://snomed.info/sctIncreased bone marrow iron
  110373000http://snomed.info/sctDecreased bone marrow iron
  110374006http://snomed.info/sctAbsent bone marrow iron
  110396000http://snomed.info/sctNo evidence of malignant neoplasm
  110440006http://snomed.info/sctBarr body present, nuclear sex female
  110441005http://snomed.info/sctBarr body absent, nuclear sex male
  110442003http://snomed.info/sctBarr body, more than one present per cell
  111001004http://snomed.info/sctGammopathy
  111407006http://snomed.info/sctHemolytic uremic syndrome
  111469006http://snomed.info/sctHemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization
  111556005http://snomed.info/sctDiabetic ketoacidosis without coma
  111571009http://snomed.info/sctCongenital atransferrinemia
  111572002http://snomed.info/sctBeta zero thalassemia non deletion type (disorder)
  111575000http://snomed.info/sctAnemia due to membrane defect
  111577008http://snomed.info/sctAnemia due to enzyme deficiency
  111579006http://snomed.info/sctHNSHA due to glutathione synthetase deficiency
  111583006http://snomed.info/sctLeukocytosis
  111584000http://snomed.info/sctReticular dysgenesis
  111585004http://snomed.info/sctNeutropenia associated with autoimmune disease
  111588002http://snomed.info/sctWhite clot syndrome
  111955002http://snomed.info/sctAnodal closure clonus
  111975006http://snomed.info/sctProlonged QT interval
  112143006http://snomed.info/sctABO group phenotype
  112144000http://snomed.info/sctBlood group A
  112149005http://snomed.info/sctBlood group B
  112211004http://snomed.info/sctGenetic translation
  112212006http://snomed.info/sctExtra chromosomal inheritance
  112631006http://snomed.info/sctSpecimen unsatisfactory for diagnosis
  113047000http://snomed.info/sctBacterial colony shape, rhizoid
  115265008http://snomed.info/sctUrinary crystal, phosphate
  115594000http://snomed.info/sctUrinary crystal, amorphous urate (finding)
  115595004http://snomed.info/sctUrinary crystal, amorphous phosphate
  115665000http://snomed.info/sctAtopic state
  115730009http://snomed.info/sctHh blood group phenotype
  115731008http://snomed.info/sctBlood group O>h< Bombay
  115732001http://snomed.info/sctBlood group O>h< Bombay Indian type
  115734000http://snomed.info/sctBlood group O>h< Bombay Reunion type
  115735004http://snomed.info/sctBlood group Para-Bombay
  115736003http://snomed.info/sctBlood group A>h<
  115737007http://snomed.info/sctBlood group B>h<
  115748000http://snomed.info/sctLewis blood group phenotype
  115749008http://snomed.info/sctLe(a-b-) phenotype
  115750008http://snomed.info/sctI blood group phenotype
  115751007http://snomed.info/scti>cord< phenotype
  115752000http://snomed.info/scti>adult< phenotype
  115753005http://snomed.info/scti>1< phenotype
  115754004http://snomed.info/scti>2< phenotype
  115755003http://snomed.info/sctI phenotype
  115756002http://snomed.info/sctI>int< phenotype
  115758001http://snomed.info/sctRhesus blood group phenotype
  115759009http://snomed.info/sctRh>null< phenotype
  115760004http://snomed.info/sctX^o^rX^o^r blood group phenotype
  115761000http://snomed.info/sctRr^-^ blood group phenotype
  115762007http://snomed.info/sctRh>mod< blood group phenotype
  115763002http://snomed.info/sctTrans weak D phenotype
  115764008http://snomed.info/sctInherited weak D phenotype
  115794002http://snomed.info/sctP blood group phenotype
  115795001http://snomed.info/sctP>1< phenotype
  115796000http://snomed.info/sctP>1<^k^ phenotype
  115797009http://snomed.info/sctP>2<^k^ phenotype
  115798004http://snomed.info/sctLandsteiner-Wiener phenotype
  115799007http://snomed.info/sctLW(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