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DO Term : congenital stationary night blindness autosomal dominant 1 [DOID:0110862] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in mutations in the RHO gene on chromosome 3q22.1.
  • synonyms:
  • CSNBAD1,
  • OMIM:610445,
  • rhodopsin-related congenital stationary night blindness,
  • 610445
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