carpal bone aplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Congenital absence of a carpal bone. (Human Phenotype Ontology, HP_0004231)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004231
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Genes

3 genes associated with the carpal bone aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
LMBR1 limb development membrane protein 1
RECQL4 RecQ protein-like 4
WNT7A wingless-type MMTV integration site family, member 7A