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Summary Literature (0)
DOID:0110714 - congenital stationary night blindness 1G

Disease Ontology Definition:A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the GNAT1 gene on chromosome 3p21.

Synonyms: congenital stationary night blindness type 1G, CSNB1G

Xenbase Genes : gnat1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014614 - cervical spinal cord white matter


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), congenital stationary night blindness (is_a)