Search Ontology:
Human Disease

amelogenesis imperfecta type 1A

Term ID
DOID:0110054
Synonyms
  • AI1A
  • amelogenesis imperfecta hypoplastic type IA
  • amelogenesis imperfecta type IA
Definition
An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the beta-3 laminin gene (LAMB3) on chromosome 1q32. (2)
References
Ontology
Human Disease   ( DOID:0110054 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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