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DO Term : congenital stationary night blindness 1F [DOID:0110864] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25.

synonyms:
OMIM:615058,
615058,
congenital stationary night blindness 1F autosomal recessive,
CSNB1F

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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