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;

Details

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]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients