Search Ontology:
Human Disease

amelogenesis imperfecta type 3A

Term ID
DOID:0110055
Synonyms
  • ADHCAI
  • AI3
  • amelogenesis imperfecta hypomineralization type
  • amelogenesis imperfecta type III
  • autosomal dominant amelogenesis imperfecta hypocalcification type
Definition
An amelogenesis imperfecta type 3 that has_material_basis_in heterozygous mutation in the FAM83H gene on chromosome 8q24. (2)
References
Ontology
Human Disease   ( DOID:0110055 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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