WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:636 central pontine myelinolysis Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  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.

1 Ontology

Name
Disease Ontology

6 Parents

Identifier Name Description
DOID:7 disease of anatomical entity A disease that manifests in a defined anatomical structure.
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:863 nervous system disease A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system.
DOID:331 central nervous system disease A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system.
DOID:3213 demyelinating disease A central nervous system disease that is characterized by damage to the myelin sheath present around nerve axons.
DOID:636 central pontine myelinolysis 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.

5 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:3213 DOID:636
is_a DOID:4 DOID:636
is_a DOID:863 DOID:636
is_a DOID:331 DOID:636
is_a DOID:7 DOID:636

1 Synonyms

Name Type
osmotic demyelination syndrome synonym