Disease #02211 (AI1E (amelogenesis imperfecta, type IE (AI1E)), OMIM:301200)

Official abbreviation AI1E
Name amelogenesis imperfecta, type IE (AI1E)
OMIM ID 301200
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene AMELX
Associated tissues -
Disease features -
Remarks -