MMP20, matrix metallopeptidase 20, 9313

N. diseases: 40; N. variants: 9
Disease: Amelogenesis Imperfecta hypomaturation type ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0399372
Disease: Amelogenesis Imperfecta hypomaturation type
Amelogenesis Imperfecta hypomaturation type 		0.300 GermlineCausalMutation disease ORPHANET MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta. 15744043 2005