proximal symphalangism (hands) Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The term proximal symphalangism refers to a bony fusion of the middle and proximal phalanges of the digits of the hand, in other words the proximal interphalangeal joint (PIJ) is missing which can be seen either on x-rays or as an absence of the proximal interphalangeal finger creases. (Human Phenotype Ontology, HP_0006152)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006152
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Genes

2 genes associated with the proximal symphalangism (hands) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NOG noggin
PTDSS1 phosphatidylserine synthase 1