joint contracture of the 5th finger Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Chronic loss of joint motion in the 5th finger due to structural changes in non-bony tissue. The term camptodactyly of the 5th finger is used if the distal and/or proximal interphalangeal joints are affected. (Human Phenotype Ontology, HP_0009183)
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5 genes associated with the joint contracture of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GJA1 gap junction protein, alpha 1, 43kDa
HOXD13 homeobox D13
LIFR leukemia inhibitory factor receptor alpha
PITX1 paired-like homeodomain 1
ZDHHC9 zinc finger, DHHC-type containing 9