Peripherin 2 - CISMeF

Preferred Label : Peripherin 2;

Symbol : PRPH2;

CISMeF acronym : PRPH2;

Type : Gene;

Alternative titles and symbols : Peripherin 2, mouse, homolog of; Rds, mouse, homolog of; Peripherin, photoreceptor type; Retinal degeneration, slow, mouse, homolog of; RDS;

Ensembl ID : ENSG00000112619;

Prefixed ID : *179605;

Details

Origin ID

179605;

UMLS CUI

C1826711;

Automatic exact mappings (from CISMeF team)
- Respiratory Distress Syndrome [NCIt concept]
- peripherin 2 [ORDO Gene]
- peripherin 2 [HGNC gene]
HGNC gene
- peripherin 2 [HGNC gene]
ORDO concept(s)
- peripherin 2 [ORDO Gene]
Phenotypes related
- Choroidal dystrophy, central areolar 2 [OMIM Phenotype]
- Fundus albipunctatus [OMIM Phenotype]
- Macular dystrophy, patterned, 1 [OMIM Phenotype]
- Macular dystrophy, vitelliform, 3 [OMIM Phenotype]
- Retinitis pigmentosa 7 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- peripherin 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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