Nephrocystin 3

Preferred Label : Nephrocystin 3;

Symbol : NPHP3;

CISMeF acronym : NPHP3;

Type : Gene;

Ensembl ID : ENSG00000113971;

Prefixed ID : *608002;

Details

Origin ID

608002;

UMLS CUI

C1417783;

Automatic exact mappings (from CISMeF team)
- nephrocystin 3 [ORDO Gene]
- nephrocystin 3 [HGNC gene]
- nephronophthisis 3 [DO Concept]
HGNC gene
- nephrocystin 3 [HGNC gene]
ORDO concept(s)
- nephrocystin 3 [ORDO Gene]
Phenotypes related
- Meckel syndrome, type 7 [OMIM Phenotype]
- Nephronophthisis 3 [OMIM Phenotype]
- Renal-hepatic-pancreatic dysplasia 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- nephrocystin 3 [HGNC gene]

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