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congenital stationary night blindness 1F

http://purl.obolibrary.org/obo/DOID_0110864

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. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

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Term info

Label

congenital stationary night blindness 1F

Synonyms

CSNB1F
congenital stationary night blindness 1F autosomal recessive

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disease_ontology

DOID:0110864

Term relations

Subclass of:

autosomal recessive disease
congenital stationary night blindness
has material basis in some autosomal recessive inheritance