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DO Term : congenital stationary night blindness 1B [DOID:0110865] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in mutation in the GRM6 gene on chromosome 5q35.
  • synonyms:
  • autosomal recessive complete congenital stationary night blindness,
  • OMIM:257270,
  • 257270,
  • CSNB1B,
  • congenital stationary night blindness 1B autosomal recessive
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents