nyctalopin - CISMeF

Preferred Label : nyctalopin;

Approved symbol HGNC : NYX;

Alias symbols HGNC : CLRP; CSNB1A;

Chromosome HGNC : Xp11.4;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000188937;

Details

Origin ID

HGNC:8082;

UMLS CUI

C1417909;

Automatic exact mappings (from CISMeF team)
- Night blindness, congenital stationary, type 1a [OMIM Phenotype]
- Nyctalopin [OMIM gene]
- nyctalopin [ORDO Gene]
OMIM gene
- Nyctalopin [OMIM gene]
Orphanet gene
- nyctalopin [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Nyctalopin [OMIM gene]

Keyword's position in hierarchy(ies) :

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