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DO Term : retinitis pigmentosa 86 [DOID:0112143] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A retinitis pigmentosa characterized by night blindness followed by progressive narrowing of visual fields and decline in visual acuity that has_material_basis_in mutation in the KIAA1549 gene on chromosome 7q34.
  • synonyms:
  • OMIM:618613,
  • 618613,
  • RP86
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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