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DO Term : amelogenesis imperfecta hypomaturation type 2A3 [DOID:0110061] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene.
  • synonyms:
  • 613211,
  • ICD10CM:K00.5,
  • AI2A3,
  • OMIM:613211,
  • amelogenesis imperfecta hypomaturation type IIA3,
  • amelogenesis imperfecta type IIA3
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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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