Search Ontology:
Human Disease

amelogenesis imperfecta type 1F

Term ID
DOID:0110065
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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