Developmental and genetic diseases

Xp22.3-p22.1   Google   OMIM   Orphanet   PubMed   [Amelogenesis imperfecta]

Amelogenesis imperfecta 1, hypoplastic type

*Gene map locus Xp22.3-p22.1
AIH1
Enamel hypoplasia, hereditary
[Clinical features: enamel anomaly; small teeth]
[Inheritance: X-linked dominant]
   
Hypoplastic amelogenesis imperfecta
    
Journal of the Canadian Dental Association
    


Search with keyword(s) Wildcard = *
          


Print this page

Edited by Aldo Campana, August 21, 2012