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DO Term : cataract 35 [DOID:0110261] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A cataract that has_material_basis_in variation in the region 19q13.
  • synonyms:
  • cataract 35, congenital nuclear,
  • OMIM:609376,
  • CATCN1,
  • CTRCT35,
  • ICD10CM:Q12.0,
  • 609376,
  • autosomal recessive congenital nuclear 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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