abnormality of the spinal meninges Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any abnormality of the spinal meninges, the system of membranes (dura mater, the arachnoid mater, and the pia mater) which envelops the spinal cord. (Human Phenotype Ontology, HP_0010303)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010303
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Genes

3 genes associated with the abnormality of the spinal meninges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FBN1 fibrillin 1
SMAD3 SMAD family member 3
TGFB2 transforming growth factor, beta 2