FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term congenital nystagmus 1 ID (Ontology) DOID:0111790 (Human Disease)
Definition A congenital nystagmus that has_material_basis_in mutation in the FRMD7 gene (FERM domain-containing-7) on chromosome Xq26.
Also Known As "congenital motor nystagmus 1" ; "NYS1" ; "X-linked infantile nystagmus 1"
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 Genes
 congenital nystagmus 1       1
 for disease ribbon | congenital nystagmus 1       1
 model of | congenital nystagmus 1       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease__
physical disorder               |
 |__congenital nystagmus________|
pathologic nystagmus            |
 |__congenital nystagmus________|
                                congenital nystagmus 1  1 rec.
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Is a X-linked recessive disease
congenital nystagmus
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Synonyms
  • "congenital motor nystagmus 1" EXACT
    "NYS1" EXACT OMO:0003012
    "X-linked infantile nystagmus 1" EXACT
Secondary IDs
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GARD:2969
MIM:310700