central pontine myelinolysis Disease Ontology Browser

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Disease Ontology Browser

central pontine myelinolysis (DOID:636)
Alliance: disease page
Synonyms: osmotic demyelination syndrome
Alt IDs: ICD10CM:G37.2, MESH:D017590, NCI:C84623, UMLS_CUI:C0206083
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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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