Search Ontology:
Human Disease

amelogenesis imperfecta type 1G

Term ID
DOID:0110066
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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