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DO Term : cataract 6 multiple types [DOID:0110229] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A cataract that has_material_basis_in heterozygous mutation in the EPHA2 gene on chromosome 1p36.
  • synonyms:
  • 116600,
  • OMIM:116600,
  • CTRCT6,
  • age related cortical cataract 2,
  • ICD10CM:Q12.0,
  • CTPP1,
  • ARCC2,
  • posterior polar cataract 1
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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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