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DO Term : cone-rod dystrophy 6 [DOID:0111011] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the GUCY2D gene on chromosome 17p13.1.
  • synonyms:
  • 601777,
  • GARD:10656,
  • retinal cone dystrophy 2,
  • OMIM:601777,
  • RCD2,
  • CORD6
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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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