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Metadata
ID DOID:0110864
Name congenital stationary night blindness 1F
Definition 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.
https://www.ncbi.nlm.nih.gov/pubmed/23246293
Xrefs

MIM:615058

Synonyms

congenital stationary night blindness 1F autosomal recessive [EXACT]

CSNB1F [EXACT]

Parent Relationships

is_a autosomal recessive disease

is_a congenital stationary night blindness

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