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DO Term : cataract 18 [DOID:0110238] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A cataract that has_material_basis_in homozygous mutation in the FYCO1 gene on chromosome 3p21.3.
  • synonyms:
  • 610019,
  • CTRCT18,
  • cataract 18 autosomal recessive,
  • autosomal recessive congenital cataract 2,
  • CATC2,
  • OMIM:610019,
  • ICD10CM:Q12.0
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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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