DISEASES

Disease-gene associations mined from literature

Human genes for amelogenesis imperfecta type 3A

Amelogenesis imperfecta type 3A [DOID:0110055]

An amelogenesis imperfecta type 3 that has_material_basis_in heterozygous mutation in the FAM83H gene on chromosome 8q24.

Synonyms:  amelogenesis imperfecta type 3A,  DOID:0110055,  ADHCAI,  AI3,  amelogenesis imperfecta hypomineralization type ...