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 2A ID (Ontology) DOID:0110871 (Human Disease)
Definition A congenital stationary night blindness that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11.23.
Also Known As "congenital stationary night blindness 2A X-linked"
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 Genes
 congenital stationary night blindness 2A       1
 for disease ribbon | congenital stationary night blindness 2A       1
 model of | congenital stationary night blindness 2A       1
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 2A  1 rec.
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Is a congenital stationary night blindness
X-linked recessive disease
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Synonyms
  • "congenital stationary night blindness 2A X-linked" EXACT
Secondary IDs
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MIM:300071