OBO ID: DOID:0110065
Term Name: amelogenesis imperfecta type 1F Search Ontology:
Synonyms:
  • AI1F
  • amelogenesis imperfecta hypoplastic type IF
  • amelogenesis imperfecta type IF
Definition: An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the ameloblastin gene (AMBN) on chromosome 4q13. https://www.ncbi.nlm.nih.gov/pubmed/24858907
References:
Ontology: Human Disease   ( DOID:0110065 )
Relationships
is a type of:
OTHER amelogenesis imperfecta type 1F PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
AMBN Amelogenesis imperfecta, type IF
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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