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DO Term : cataract 9 multiple types [DOID:0110266] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A cataract that has_material_basis_in autosomal recessive or autosomal dominant inheritance of heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22.
  • synonyms:
  • 604219,
  • autosomal recessive congenital cataract 1,
  • CATC1,
  • OMIM:604219,
  • CTRCT9,
  • cataract 9 multiple types with or without microcornea,
  • 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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