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DO Term : congenital stationary night blindness autosomal dominant 2 [DOID:0110863] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the PDE6B gene on chromosome 4p16.
  • synonyms:
  • CSNBAD2,
  • OMIM:163500,
  • 163500,
  • Rambusch type congenital stationary night blindness
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Disease

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Ontology

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Ontology Term --> Direct parents





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