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NCIm Version: 201808 (Browser Version 2.9, using LexEVS 6.5.1)
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Skin Diseases, Genetic (CUI C0037277) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0037277

Semantic Type: Disease or Syndrome

MSH Definition: Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.

Synonyms & Abbreviations: (see Synonym Details)
Disease, Genetic Skin
Diseases, Genetic Skin
GENET SKIN DIS
Genetic Skin Diseases
Genetic Skin Disease
Genodermatosis (disorder)
Genodermatosis
SKIN DIS GENET
Skin Disease, Genetic
Skin Diseases, Genetic [Disease/Finding]
Skin Diseases, Genetic

External Source Codes:  (none)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AN GEN or unspecified; prefer specifics; DF: SKIN DIS GENET MSH
AQL BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI MSH
CASE_SIGNIFICANCE_ID 900000000000448009 SNOMEDCT_US
CHARACTERISTIC_TYPE_ID 900000000000011006 SNOMEDCT_US
CTV3ID X50H0 SNOMEDCT_US
DC 1 MSH
DEFINITION_STATUS_ID 900000000000074008 SNOMEDCT_US
DX 19980101 MSH
EFFECTIVE_TIME 20020131 SNOMEDCT_US
HN 98; use explode 1970-97 MSH
MDA 19990101 MSH
MESH_DEFINITION Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism. NDFRT
MESH_DUI D012873 NDFRT
MESH_NAME Skin Diseases, Genetic NDFRT
MESH_UI M0019934 NDFRT
MMR 20150618 MSH
MN C16.320.850 MSH
MN C17.800.827 MSH
MODIFIER_ID 900000000000451002 SNOMEDCT_US
NDFRT_KIND DISEASE_KIND NDFRT
NUI N0000002763 NDFRT
PM 98 MSH
RXAUI 3165192 RXNORM
RXAUI 3238593 RXNORM
RXAUI 3238594 RXNORM
RXCUI 986094 RXNORM
SNOMED_CID 239001006 NDFRT
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS Q82.8 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~Q82.8 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS Q82.8 | DESCENDANTS NOT EXHAUSTIVELY MAPPED SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~Q82.8 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~X50H0 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
TERMUI T037953 MSH
TERMUI T037954 MSH
TH NLM (1966) MSH
TH NLM (1998) MSH
TYPE_ID 900000000000003001 SNOMEDCT_US
TYPE_ID 900000000000013009 SNOMEDCT_US

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C0037277

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