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DO Term : X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 [DOID:0110059] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region.
  • synonyms:
  • 301201,
  • OMIM:301201,
  • amelogenesis imperfecta type IE X-linked 2,
  • AIH3,
  • X-linked enamel hypoplasia,
  • ICD10CM:K00.5,
  • amelogenesis imperfecta 3 hypoplastic type
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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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