absent ulna Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Missing ulna bone associated with congenital failure of development. (Human Phenotype Ontology, HP_0003982)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003982
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4 genes associated with the absent ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
LMBR1 limb development membrane protein 1
TBX3 T-box 3
WNT7A wingless-type MMTV integration site family, member 7A