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DO Term : cone-rod dystrophy 2 [DOID:0111005] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the CRX gene on chromosome 19q13.
  • synonyms:
  • 120970,
  • CRD2,
  • GARD:6145,
  • RCRD2,
  • cone-rod retinal dystrophy 2,
  • retinal cone-rod dystrophy 2,
  • OMIM:120970,
  • CORD2
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Ontology Term --> Direct parents





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