USH1G Gene - CISMeF

Preferred Label : USH1G Gene;

NCIt synonyms : Usher Syndrome 1G (Autosomal Recessive) Gene; USH1G;

CISMeF acronym : USH1G;

NCIt definition : This gene plays a role in both sight and hearing.;

Details

Origin ID

C114406;

UMLS CUI

C1424214;

Automatic exact mappings (from CISMeF team)
- USH1 protein network component sans [ORDO Gene]
- Ush1 protein network component sans [OMIM gene]
- Usher syndrome type 1G [DO Concept]
- Usher syndrome, type ig [OMIM Phenotype]
HGNC gene
- USH1 protein network component sans [HGNC gene]
OMIM relation
- Ush1 protein network component sans [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- USH1 protein network component sans [HGNC gene]
- Ush1 protein network component sans [OMIM gene]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Reference Gene Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_encodes_gene_product
- Usher Syndrome Type-1G Protein [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Eye Development [NCIt concept]
- Hearing [NCIt concept]
- Sight [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

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