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DO Term : retinitis pigmentosa 6 [DOID:0110413] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A retinitis pigmentosa that has_material_basis_in variation in the chromosome region Xp21.3-p21.2.
  • synonyms:
  • RP6,
  • MESH:C564065,
  • 312612,
  • ICD10CM:H35.5,
  • OMIM:312612
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents