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DO Term : cone-rod dystrophy 5 [DOID:0111010] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A cone-rod dystrophy that has_material_basis_in mutation in the PITPNM3 gene in chromosome region 17p13.2-p13.1.
  • synonyms:
  • OMIM:600977,
  • 600977,
  • CORD5,
  • MESH:C563415
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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





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