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Metadata
ID DOID:0110870
Name congenital stationary night blindness 1A
Definition A congenital stationary night blindness that has_material_basis_in mutation in the NYX gene on chromosome Xp11.4.
https://www.ncbi.nlm.nih.gov/pubmed/9662400
Xrefs

MIM:310500

Synonyms

complete CSNB X-linked [EXACT]

congenital stationary night blindness 1A X-linked [EXACT]

congenital stationary night blindness with myopia [EXACT]

CSNB1A [EXACT]

hemeralopia-myopia [EXACT]

myopia-night blindness [EXACT]

NBMI [EXACT]

Parent Relationships

is_a congenital stationary night blindness

is_a X-linked recessive disease

Subclass Logical Relationships

has material basis in some X-linked recessive inheritance

disease has basis in some Abnormality of prenatal development or birth

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