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DO Term : cataract 1 multiple types [DOID:0110231] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A cataract that has_material_basis_in heterozygous mutation in the gene encoding the alpha-8 subunit of the gap junction protein (GJA8) on chromosome 1q21.
  • synonyms:
  • CTRCT1,
  • OMIM:116200,
  • ICD10CM:Q12.0,
  • CZP1,
  • CAE1,
  • zonular pulverulent cataract 1,
  • 116200,
  • cataract 1, multiple types, with or without microcornea,
  • Duffy linked cataract
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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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