FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term congenital stationary night blindness 1A ID (Ontology) DOID:0110870 (Human Disease)
Definition A congenital stationary night blindness that has_material_basis_in mutation in the NYX gene on chromosome Xp11.4.
Also Known As "complete CSNB X-linked" ; "congenital stationary night blindness 1A X-linked" ; "congenital stationary night blindness with myopia" (for all, see Synonyms field below)
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 Genes
 congenital stationary night blindness 1A       2
 for disease ribbon | congenital stationary night blindness 1A       2
 model of | congenital stationary night blindness 1A       2
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease_____________
physical disorder                          |
 |__congenital stationary night blindness__|
hereditary night blindness                 |
 |__congenital stationary night blindness__|
                                           congenital stationary night blindness 1A  2 rec.
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Is a congenital stationary night blindness
X-linked recessive disease
Part of
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Synonyms
  • "complete CSNB X-linked" EXACT
    "congenital stationary night blindness 1A X-linked" EXACT
    "congenital stationary night blindness with myopia" EXACT
    "CSNB1A" EXACT OMO:0003012
    "hemeralopia-myopia" EXACT
    "myopia-night blindness" EXACT
    "NBMI" EXACT OMO:0003012
Secondary IDs
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MIM:310500