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DO Term : congenital stationary night blindness 1D [DOID:0110868] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the SLC24A1 gene on chromosome 15q22.
  • synonyms:
  • OMIM:613830,
  • congenital stationary night blindness 1D autosomal recessive,
  • CSNB1D,
  • 613830
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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





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