Metadata | |
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ID | DOID:0110871 |
Name | congenital stationary night blindness 2A |
Definition | A congenital stationary night blindness that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11.23. https://www.ncbi.nlm.nih.gov/pubmed/9662399 |
Xrefs | |
Synonyms |
congenital stationary night blindness 2A X-linked [EXACT] |
Parent Relationships | |
Subclass Logical Relationships |
has material basis in some X-linked recessive inheritance disease has basis in some Abnormality of prenatal development or birth |