ZFIN Human Disease: congenital stationary night blindness autosomal dominant 1

OBO ID: DOID:0110862

Term Name:	congenital stationary night blindness autosomal dominant 1		Search Ontology:
Synonyms:	CSNBAD1 rhodopsin-related congenital stationary night blindness
Definition:	A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in mutations in the RHO gene on chromosome 3q22.1. https://www.ncbi.nlm.nih.gov/pubmed/7846071
References:	OMIM:610445
Ontology:	Human Disease ( DOID:0110862 )

Relationships

is a type of:	autosomal dominant disease congenital stationary night blindness autosomal dominant disease congenital stationary night blindness Show first 5 Terms

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
RHO	rho	Night blindness, congenital stationary, autosomal dominant 1	610445

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None