short middle phalanx of the 5th finger Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment (hypoplasia) of the middle phalanx of the fifth finger. (Human Phenotype Ontology, HP_0004220)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004220
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Genes

8 genes associated with the short middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GATA1 GATA binding protein 1 (globin transcription factor 1)
GJA1 gap junction protein, alpha 1, 43kDa
H19 H19, imprinted maternally expressed transcript (non-protein coding)
HOXD13 homeobox D13
RBBP8 retinoblastoma binding protein 8
ROR2 receptor tyrosine kinase-like orphan receptor 2
RUNX2 runt-related transcription factor 2
WNT5A wingless-type MMTV integration site family, member 5A