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DO Term : congenital stationary night blindness 1C [DOID:0110867] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital stationary night blindness characterized by autosomal recessive that has_material_basis_in homozygous or compound heterozygous mutation in the TRPM1 gene on chromosome 15q13-q14.

synonyms:
613216,
CSNB1C,
OMIM:613216,
congenital stationary night blindness 1C autosomal recessive

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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