Juvenile primary lateral sclerosis Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Juvenile primary lateral sclerosis (JPLS) is a very rare motor neuron disease characterized by progressive upper motor neuron dysfunction leading to loss of the ability to walk with wheelchair dependence, and subsequently, loss of motor speech production. (Orphanet Rare Disease Ontology, Orphanet_247604)
External Link http://www.omim.org/entry/606353
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Genes

1 genes associated with the Juvenile primary lateral sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)