mesomelic arm shortening Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Shortening of the middle parts of the arm in relation to the upper and terminal segments. (Human Phenotype Ontology, HP_0005011)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005011
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Genes

1 genes associated with the mesomelic arm shortening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FLNA filamin A, alpha