0.1.1 - ci-build

This page is part of the MatchSync Implementation Guide (v0.1.0: Release Draft) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions

CodeSystem: NMDP Disease Code System (Experimental)

Official URL: http://terminology.nmdp.org/codesystem/disease Version: 0.1.1
Active as of 2024-11-11 Computable Name: NMDPDiseaseCS

Copyright/Legal: National Marrow Donor Program

Code System for NMDP diseases

This Code system is referenced in the content logical definition of the following value sets:

Generated Narrative: CodeSystem nmdp-disease-cs

This case-sensitive code system http://terminology.nmdp.org/codesystem/disease defines the following codes:

CodeDisplay
ABL ACUTE BILINEAGE LEUKEMIA
AISA ACQ IDIOPATH SIDERBLASTIC ANEM
ALD ADRENOLEUKODYSTROPHY
ALL ACUTE LYMPHOBLASTIC LEUKEMIA
AMCL ACUTE MAST CELL LEUKEMIA
AMEGCT AMEGAKARYOCY/CONGENTIAL THROM
AML ACUTE MYELOGENOUS LEUKEMIA
ASPGL ASPARTYL GLUCOSAMINIDASE
AT ATAXIA-TELANGIECTASIA
AUL ACUTE UNDIFFERENTIATED LEUK-MO
BGLUD BETA-GLUCURONIDASE DEFICIENCY
BLSYND BARE LYMPHOCYTE SYNDROME
BRCA BREAST CANCER
BTHAL BETA THALASSEMIA MAJOR
C-HHYP CARTILAGE-HAIR HYPOPLASIA
CGD CHRONIC GRANULOMATOUS DISEASE
CID COMBINED IMMUNODEFICIENCY
CLL CHRONIC LYMPHOCYTIC LEUKEMIA
CML CHRONIC MYELOGENOUS LEUKEMIA
CMML CHRONIC MYELOMONOCYTIC LEUK
CNSCA CENTRAL NERVOUS SYSTEM TUMORS
DIGRGE DI GEORGE SYNDROME
ETC ESSENTIAL THROMOBOCYTHEMIA
EWINGS EWINGS SARCOMA
FA FANCONI ANEMIA
FEL FAMILIAL ERYTHROPHAGOCYTIC
FUCOSI FUCOSIDOSIS
GAUCHR GAUCHER'S DISEASE
GLTROM GLANZMANNS THROMBASTHENIA
GLUCST GLUCOSE STORAGE DISEASE
HCL HAIRY CELL LEUKEMIA
HISX HISTIOCYTOSIS-X
HIV HIV INFECTION
HL HODGKINS LYMPHOMA
HPGC HEMOPHAGOCYTOSIS
HUNTER HUNTER SYNDROME (MPS-II)
HURLER HURLER SYNDROME (MPS-IH)
ICELL I-CELL DISEASE
IMDNP IMMUNE DEFICIENCY + NEUTROPEN
JCML JUVENILE CHRONIC MYELOGENOUS
KOSTMN KOSTMANN'S AGRANULOCYTOSIS
KRABBE KRABBE DISEASE
LAD LEUKOCYTE ADHESION DEFICIENCY
LN LESCH-NYHAN
LNS LESCH-NYHAN
LYSOST LYSOSOMAL STORAGE DISEASE
MANNO MANNOSIDOSIS
MARLAM MAROTEAUX-LAMY (MPS-VI)
MDS MYELODYSPLASTIC DISORDER
MFMM MYELOFIBRO MYELOID METAPLASIA
MLD METACHROMATIC LEUKODYSTROPHY
MM MULTIPLE MYELOMA
MORQUA MORQUIO A - MPS IVA
MORQUB MORQUIO B - MPS IVB
MORQUO MORQUIO (MPS-IV)
MPS MUCOPOLYSACCHARIDOSIS (MPS-V)
N-P NEIMAN-PICK DISEASE
NB NEUROBLASTOMA
NCL1 ENZYME NCL 1
NCL2 ENZYME NCL 2
NEUTAD NEUTROPHIL ACTIN DEFICIENCY
NEUTD CHEDIAK-HIGASHI SYNDROME
NHL NON-HODGKINS LYMPHOMA
OCID OTHR COMBINED IMMUNODEFICIENCY
OHIS OTHER HISTIOCYTIC DISORDERS
OIEA OTH ERYTHROCYT DIFFERENTIATION
OIIS OTHER IMMUNE SYSTEM
OIMD OTH INHER METABOLISM DISORD
OIMDL OTH MUCOLIPIDOSES
OIMDP OTH MUCOPOLYSACCHARIDOSIS
OIPA OTH ABNORMALITIES OR PLATELETS
OMDS OTHER MYELODYSPLASTIC DISORDER
OMF OTHER MYLEOFIBROSIS/MYLEOSCLER
OMMEN OMMEN'S SYNDROME
OMS OTH MALIGNANCY, SPECIFY
OND OTHER NON-MALIGNANT DISEASE
OOL OTHER LEUKEMIA SPECIFY
OPCD OTHER PLASMA CELL DISORDER
OSCID OTHER SCID
OST OSTEOPETROSIS
OTHHGP OTHER HEMOGLOBINOPATHY
PCL PLASMA CELL LEUKEMIA
PHILLY PROLYMPHOCYTIC LEUKEMIA
PNH PAROXYSMAL NOCTURNAL HEMOGLOB
PV POLYCYTHEMIA VERA
RA REFRACTORY ANEMIA (RA)
RAEB REFRACT ANEMIA-EXCESS BLASTS
RAEBIT REFRACT ANEMIA-EX. BLAST TRAN
RCA PURE RED CELL APLASIA
RCC RENAL CELL CARCINOMA
RETDG RETICULAR DYSGENESIS
SAA SEVERE APLASTIC ANEMIA
SANFIA SANFILIPPO A - MPS IIIA
SANFIB SANFILIPPO B - MPS IIIB
SANFIC SANFILIPPO C - MPS IIIC
SANFID ANFILIPPO D - MPS IIID
SANFIL SANFILLIPPO (MPS-III)
SCA SICKLE CELL ANEMIA
SCHEIE SCHEIE SYNDROME (MPS-IS)
SCID SEVERE COMBINED IMMUNODEF