Disease #02211 (AI-1E (amelogenesis imperfecta, type IE (AI-1E)), OMIM:301200)

Official abbreviation AI-1E
Name amelogenesis imperfecta, type IE (AI-1E)
OMIM ID 301200
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene AMELX
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 27
LOVD software ©2004-2021 Leiden University Medical Center 		There are currently no updates.