Usher syndrome, type ih

Preferred Label : Usher syndrome, type ih;

Symbol : USH1H;

CISMeF acronym : USH1H;

Type : Phenotype or locus, molecular basis unknown;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of Usher syndrome type I, see USH1 (276900).;

Prefixed ID : %612632;

Details

Origin ID

612632;

UMLS CUI

C2675458;

Automatic exact mappings (from CISMeF team)
- Usher syndrome 1H (autosomal recessive) [HGNC gene]
- Usher syndrome 1H (autosomal recessive) [ORDO Gene]
- Usher syndrome type 1 [ORDO Disease]
- Usher syndrome type 1H [DO Concept]
Broader ORDO disease(s)
- Usher syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- usher syndrome, type IH [MeSH concept]
- usher syndrome, type IH [MeSH Supplementary Concept]
DO Cross reference
- Usher syndrome type 1H [DO Concept]
ORDO concept(s)
- Usher syndrome [ORDO Disease]
- Usher syndrome type 1 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- usher syndrome, type IH [MeSH Supplementary Concept]
- usher syndrome, type IH [MeSH concept]

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