progressive inability to walk Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002505
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Genes

10 genes associated with the progressive inability to walk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAR adenosine deaminase, RNA-specific
AP4S1 adaptor-related protein complex 4, sigma 1 subunit
C10ORF2 chromosome 10 open reading frame 2
CLN3 ceroid-lipofuscinosis, neuronal 3
ERBB4 erb-b2 receptor tyrosine kinase 4
FAM126A family with sequence similarity 126, member A
GDAP1 ganglioside induced differentiation associated protein 1
SLC9A6 solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
SUCLA2 succinate-CoA ligase, ADP-forming, beta subunit
TK2 thymidine kinase 2, mitochondrial