hypertrichosis 1 (universalis, congenital)

Preferred Label : hypertrichosis 1 (universalis, congenital);

Obsolete resource : true;

Approved symbol HGNC : HTC1;

Name synonyms HGNC : Ambras syndrome;

Chromosome HGNC : 8;

Locus type HGNC : phenotype;

Détails

Origin ID

HGNC:5277;

UMLS CUI

C1415795;

Automatic exact mappings (from CISMeF team)
- Hypertrichosis universalis congenita, ambras type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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