Potassium channel, inwardly rectifying, subfamily j, member 13

Preferred Label : Potassium channel, inwardly rectifying, subfamily j, member 13;

Symbol : KCNJ13;

CISMeF acronym : KCNJ13;

Type : Gene;

Alternative titles and symbols : Inwardly rectifying potassium channel kir7.1;

Ensembl ID : ENSG00000115474;

Prefixed ID : *603208;

Détails

Origin ID

603208;

UMLS CUI

C1416580;

Automatic exact mappings (from CISMeF team)
- potassium inwardly rectifying channel subfamily J member 13 [HGNC gene]
- potassium inwardly rectifying channel subfamily J member 13 [ORDO Gene]
HGNC gene
- potassium inwardly rectifying channel subfamily J member 13 [HGNC gene]
ORDO concept(s)
- potassium inwardly rectifying channel subfamily J member 13 [ORDO Gene]
Phenotypes related
- Leber congenital amaurosis 16 [OMIM Phenotype]
- Vitreoretinal degeneration, snowflake type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- potassium inwardly rectifying channel subfamily J member 13 [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients