2 results
Disease Genes: prx-10 (Cel)
Source: DOID:700
Definition: An inherited metabolic disorder that involves mitochondrial metabolism dysfunction.
Genes: prx-10 (Cel)

Source: DOID:480
Definition: A brain disease that is characterized by a clinical syndrome of either hyperkinetic movement or hyperkinetic movement unrelated to weakness or spasticity.
Genes: prx-10 (Cel)