abnormality of the medullary cavity of the long bones Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the medullary cavity (medulla, innermost part), which is the central cavity of bone shafts where red bone marrow and/or yellow bone marrow (adipose tissue) is stored. (Human Phenotype Ontology, HP_0100253)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100253
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Genes

2 genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FAM111A family with sequence similarity 111, member A
MTAP methylthioadenosine phosphorylase