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DO Term : retinitis pigmentosa 7 [DOID:0110383] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A retinitis pigmentosa that has_material_basis_in mutation in the PRPH2 gene on chromosome 6p21.
  • synonyms:
  • RP7,
  • ICD10CM:H35.5,
  • MESH:C564284,
  • OMIM:608133,
  • 608133
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Disease

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Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents





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