aplasia/hypoplasia of the palmar creases Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the palmar creases. (Human Phenotype Ontology, HP_0010488)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010488
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6 genes associated with the aplasia/hypoplasia of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DOK7 docking protein 7
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
PIEZO2 piezo-type mechanosensitive ion channel component 2
PLOD3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
RAPSN receptor-associated protein of the synapse
SLC39A13 solute carrier family 39 (zinc transporter), member 13