cutaneous syndactyly of toes Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A soft tissue continuity in the anteroposterior axis between adjacent foot digits that involves at least half of the proximodistal length of one of the two involved digits; or, a soft tissue continuity in the A/P axis between two digits of the foot that does not meet the prior objective criteria. (Human Phenotype Ontology, HP_0010621)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010621
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Genes

5 genes associated with the cutaneous syndactyly of toes 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
MYH8 myosin, heavy chain 8, skeletal muscle, perinatal
NOG noggin
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)
PVRL4 poliovirus receptor-related 4