aplasia of the phalanges of the hand Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of one or more of the phalanges of the hand. (Human Phenotype Ontology, HP_0009802)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009802
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Genes

8 genes associated with the aplasia of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BMPR1B bone morphogenetic protein receptor, type IB
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GJA1 gap junction protein, alpha 1, 43kDa
LMBR1 limb development membrane protein 1
LMNA lamin A/C
MEGF8 multiple EGF-like-domains 8