OBO ID: DOID:0110055
Term Name: amelogenesis imperfecta type 3A Search Ontology:
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 amelogenesis imperfecta type 3A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FAM83H Amelogenesis imperfecta, type IIIA 130900
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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