OBO ID: DOID:0110066
Term Name: amelogenesis imperfecta type 1G Search Ontology:
Synonyms:
  • AI1G
  • AIGFS
  • amelogenesis imperfecta and gingival fibromatosis syndrome
  • amelogenesis imperfecta hypoplastic with nephrocalcinosis
  • amelogenesis imperfecta type IG
  • enamel-renal syndrome
  • enamel-renal-gingival syndrome
  • ERS
Definition: An amelogenesis imperfecta that has_material_basis_in homozygous or compound heterozygous mutation in the FAM20A gene on chromosome 17q24. (2)
References:
Ontology: Human Disease   ( DOID:0110066 )
Relationships
is a type of:
OTHER amelogenesis imperfecta type 1G PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FAM20A Amelogenesis imperfecta, type IG (enamel-renal syndrome) 204690
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.