Dupuytren Contracture Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the hand resulting from contracture of the palmar fascia with a fixed flexion deformity of the metacarpophalangeal (MCP) joints and the proximal interphalangeal (PIP) joints. (Human Phenotype Ontology, HP_0005679)
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10 genes associated with the Dupuytren Contracture phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial)
DHDH dihydrodiol dehydrogenase (dimeric)
EPDR1 ependymin related 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
RSPO2 R-spondin 2
SFRP4 secreted frizzled-related protein 4
SULF1 sulfatase 1
WNT2 wingless-type MMTV integration site family member 2
WNT4 wingless-type MMTV integration site family, member 4
WNT7B wingless-type MMTV integration site family, member 7B