DISEASES

Disease-gene associations mined from literature

Human genes for amelogenesis imperfecta hypomaturation type 2A2

Amelogenesis imperfecta hypomaturation type 2A2 [DOID:0110060]

An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the matrix metalloproteinase-20 gene (MMP20).

Synonyms:  amelogenesis imperfecta hypomaturation type 2A2,  DOID:0110060,  AI2A2,  amelogenesis imperfecta hypomaturation type IIA2,  amelogenesis imperfecta pigmented hypomaturation type 2 ...