Usher syndrome 1H (autosomal recessive)

Preferred Label : Usher syndrome 1H (autosomal recessive);

Obsolete resource : true;

Approved symbol HGNC : USH1H;

Chromosome HGNC : 15q22-q23;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:22433;

UMLS CUI

C2681110;

Automatic exact mappings (from CISMeF team)
- Usher syndrome, type ih [OMIM Phenotype]
Orphanet gene
- Usher syndrome 1H (autosomal recessive) [ORDO Gene]
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