motor deterioration Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Loss of previously present motor (i.e., movement) abilities. (Human Phenotype Ontology, HP_0002333)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002333
Similar Terms
Downloads & Tools

Genes

6 genes associated with the motor deterioration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CLN5 ceroid-lipofuscinosis, neuronal 5
CLN6 ceroid-lipofuscinosis, neuronal 6, late infantile, variant
GALC galactosylceramidase
HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
MECP2 methyl CpG binding protein 2
RBM28 RNA binding motif protein 28