FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term congenital nystagmus 2 ID (Ontology) DOID:0111792 (Human Disease)
Definition A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 6p12.
Also Known As "autosomal dominant congenital nystagmus 2" ; "congenital motor nystagmus 2" ; "NYS2"
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autosomal genetic disease
 |__autosomal dominant disease__
physical disorder               |
 |__congenital nystagmus________|
pathologic nystagmus            |
 |__congenital nystagmus________|
                                congenital nystagmus 2
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Is a autosomal dominant disease
congenital nystagmus
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Synonyms
  • "autosomal dominant congenital nystagmus 2" EXACT
    "congenital motor nystagmus 2" EXACT
    "NYS2" EXACT OMO:0003012
Secondary IDs
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GARD:9599
MIM:164100