FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term central pontine myelinolysis ID (Ontology) DOID:636 (Human Disease)
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.
Also Known As "osmotic demyelination syndrome"
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 Genes
 for disease ribbon | migraine       1
 model of | migraine       1
Spanning Tree (Parents/Children)
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  central nervous system disease
   |__demyelinating disease
       |__central pontine myelinolysis
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Is a demyelinating disease
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Synonyms
  • "osmotic demyelination syndrome" EXACT
Secondary IDs
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GARD:8749
ICD10CM:G37.2
MESH:D017590
NCI:C84623
SNOMEDCT_US_2023_03_01:6807001
UMLS_CUI:C0206083