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DOID:636 - central pontine myelinolysis
Disease Ontology Definition: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: osmotic demyelination syndrome
Echinobase Genes

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
demyelinating disease (is_a)