Human genes for central pontine myelinolysis
Central pontine myelinolysis [DOID:636]
A demyelination disease that is characterized by severe damage to the myelin sheath of the pons' nerve cells and has_symptom acute paralysis, has_symptom dysphagia, and has_symptom dysarthria.
Synonyms: central pontine myelinolysis, central pontine myelinolysises, DOID:636, osmotic demyelination syndrome, osmotic demyelination disease ...