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DO Term : amelogenesis imperfecta type 3A [DOID:0110055] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An amelogenesis imperfecta type 3 that has_material_basis_in heterozygous mutation in the FAM83H gene on chromosome 8q24.
  • synonyms:
  • amelogenesis imperfecta hypomineralization type,
  • amelogenesis imperfecta type III,
  • autosomal dominant amelogenesis imperfecta hypocalcification type,
  • OMIM:130900,
  • ICD10CM:K00.5,
  • ADHCAI,
  • 130900
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Disease

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Ontology

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Ontology Term --> Direct parents





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