Disease #04553 (AI1A (amelogenesis imperfecta, type IA (AI1A)), OMIM:104530)

Official abbreviation AI1A
Name amelogenesis imperfecta, type IA (AI1A)
OMIM ID 104530
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene LAMB3
Associated tissues -
Disease features -
Remarks -

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