Home Page
References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 01-09-2021
Symbol AI1F
Location 4q13.3
Name amelogenesis imperfecta, type IF
Corresponding gene AMBN
Main clinical features
  • characterized by hypoplastic enamel of the primary and secondary dentition; teeth may appear rough and discolored, and the tooth enamel may be absent, pitted, or of varying thickness
  • Genetic determination autosomal recessive
    Function/system disorder digestive tract/liver and annex
    Type disease
    Remark(s)