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DO Term : cataract 15 multiple types [DOID:0110251] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A cataract that has_material_basis_in heterozygous mutation in the MIP gene on chromosome 12q13.
  • synonyms:
  • OMIM:615274,
  • CTRCT15,
  • ICD10CM:Q12.0,
  • 615274
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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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