Amelogenesis imperfecta pigmented hypomaturation type Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C538242
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Genes

2 genes/proteins associated with the disease Amelogenesis imperfecta pigmented hypomaturation type from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
KLK4 kallikrein-related peptidase 4 2.88009
MMP20 matrix metallopeptidase 20 2.88009