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Wernicke Encephalopathy

Disease ID: disease_node_7971

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Dbxref	ICD10CM:E51.2, MESH:D014899, SNOMEDCT_US_2023_03_01:190627001, UMLS_CUI:C0043121
Subclassof	DOID_936
Data Source	DOID, MESH
Synonyms	Wernicke's disease, Wernicke's encephalopathy
Mesh Id	D014899
Mesh Label	Wernicke Encephalopathy
Mesh Subclassof	D019973, D001928, D013832
Doid Label	Wernicke encephalopathy
Doid Description	A brain disease that is characterized by the presence of neurological symptoms of ophthalmoplegia, ataxia, and confusion caused by biochemical lesions of the central nervous system after exhaustion of B-vitamin reserves, in particular thiamine (vitamin B1).
Has Symptom	SYMP_0000016, SYMP_0000005
Disease Node Id	disease_node_7971
Doid Id	DOID_2384
Label	Wernicke Encephalopathy

Outgoing r'ship HAS_SYMPTOM to/from Confusion(ID:disease_node_2215;disease_node_21603) (Disease)
Outgoing r'ship HAS_SYMPTOM to/from Ataxia(ID:disease_node_1424;disease_node_21621) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Brain Diseases(ID:disease_node_1682) (Disease)

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