Disease #04527

Official abbreviation AI-1H
Name amelogenesis imperfecta, type IH (AI-1H)
OMIM ID 616221
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ITGB6
Associated tissues -
Disease features -
Remarks -