OBO ID: DOID:0110054
Term Name: amelogenesis imperfecta type 1A Search Ontology:
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 amelogenesis imperfecta type 1A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LAMB3 Amelogenesis imperfecta, type IA 104530
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.