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DO Term : retinitis pigmentosa 10 [DOID:0110388] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A retinitis pigmentosa that has_material_basis_in mutation in the IMPDH1 gene on chromosome 7q32.
  • synonyms:
  • 180105,
  • ICD10CM:H35.5,
  • RP10,
  • OMIM:180105,
  • MESH:C566715
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Disease

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Ontology Term --> Direct parents





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