Clarin 1 - CISMeF

Preferred Label : Clarin 1;

Symbol : CLRN1;

CISMeF acronym : CLRN1;

Type : Gene;

Alternative titles and symbols : Ush3a gene; USH3A; USH3;

Ensembl ID : ENSG00000163646;

Prefixed ID : *606397;

Details

Origin ID

606397;

UMLS CUI

C1824756;

Automatic exact mappings (from CISMeF team)
- Usher syndrome type 3 [DO Concept]
- Usher syndrome type 3 [ORDO Disease]
- Usher syndrome type 3A [DO Concept]
Currated CISMeF NLP mapping
- CLRN1 [LOINC component]
- clarin 1 [ORDO Gene]
- clarin 1 [HGNC gene]
HGNC gene
- clarin 1 [HGNC gene]
ORDO concept(s)
- clarin 1 [ORDO Gene]
Phenotypes related
- Retinitis pigmentosa 61 [OMIM Phenotype]
- Usher syndrome, type iiia [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CLRN1 [LOINC component]
- clarin 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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