aplasia of the middle phalanx of the hand Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of one or more middle phalanx of a finger. (Human Phenotype Ontology, HP_0010239)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010239
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6 genes associated with the aplasia of the middle phalanx of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GJA1 gap junction protein, alpha 1, 43kDa
LMNA lamin A/C
MEGF8 multiple EGF-like-domains 8