hypertrichosis 2 (generalized, congenital)

Preferred Label : hypertrichosis 2 (generalized, congenital);

Obsolete resource : true;

Approved symbol HGNC : HTC2;

Alias symbols HGNC : CGH; HCG;

Chromosome HGNC : Xq27.1;

Locus type HGNC : phenotype;

Détails

Origin ID

HGNC:5278;

UMLS CUI

C1415796;

Automatic exact mappings (from CISMeF team)
- Hypertrichosis, congenital generalized, 2 [OMIM Phenotype]
NCIt concept
- HTC2 Gene [NCIt concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HTC2 Gene [NCIt concept]
- HTC2 gene [LOINC component]

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