usher syndrome, type IG

Preferred Label : usher syndrome, type IG;

MeSH note : also known as USH1G; associated with mutation in SANS gene;

Origin ID

C564643;

UMLS CUI

C1847089;

Automatic exact mappings (from CISMeF team)
- Usher syndrome type 1G [DO Concept]
Currated CISMeF NLP mapping
- Usher syndrome type Ig [Disease (Nov.)]
- Usher syndrome, type ig [OMIM Phenotype]
MeSH term(s) associated for indexing
- usher syndromes [MeSH Descriptor]
Record concept(s)
- usher syndrome, type IG [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Usher syndrome type Ig [Disease (Nov.)]
- Usher syndrome, type ig [OMIM Phenotype]