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DO Term : retinitis pigmentosa 19 [DOID:0110354] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A retinitis pigmentosa that has_material_basis_in mutation in the ABCA4 gene on chromosome 1p22.
  • synonyms:
  • 601718,
  • MESH:C566637,
  • OMIM:601718,
  • RP19,
  • ICD10CM:H35.5
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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