oligodactyly (hands) Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect resulting in the presence of fewer than the normal number of fingers. (Human Phenotype Ontology, HP_0001180)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001180
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8 genes associated with the oligodactyly (hands) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHD7 chromodomain helicase DNA binding protein 7
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
NIPBL Nipped-B homolog (Drosophila)
PORCN porcupine homolog (Drosophila)
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SMOC1 SPARC related modular calcium binding 1
WNT10B wingless-type MMTV integration site family, member 10B
WNT7A wingless-type MMTV integration site family, member 7A