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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Brain Diseases, Metabolic (D001928)
Parent Node: Demyelinating Diseases (D003711)
..Starting node ..Marchiafava-Bignami Disease (D054319)
Child Nodes:
Sister Nodes:
..Boylan Dew Greco syndrome (C537083)
..CAMFAK syndrome (C537965)
..Demyelinating Autoimmune Diseases, CNS (D020278) 15
..Groll Hirschowitz syndrome (C537305)
..Hamano Tsukamoto syndrome (C535625)
..Hereditary Central Nervous System Demyelinating Diseases (D020279) 29
..Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response (C537159)
..Leukoencephalopathy, Progressive Multifocal (D007968)
..Marchiafava-Bignami Disease (D054319)
..Myelinolysis, Central Pontine (D017590)
..Ophthalmoplegic Migraine (D060486)
..Polyradiculoneuropathy (D011129) 18
..Subacute Combined Degeneration (D052879)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6784
Name:	Marchiafava-Bignami Disease
Definition:	A neurodegenerative condition that is characterized by demyelination or necrosis of the CORPUS CALLOSUM. Symptoms include DEPRESSION; PARANOIA; DEMENTIA; SEIZURES; and ATAXIA which can progress to COMA and death in a few months. Marchiafava-Bignami syndrome is seen often in alcoholics but has been found in non-alcoholics as well.
Alternative IDs:
ParentIDs:	MESH:D001928\|MESH:D003711
TreeNumbers:	C10.228.140.163.510 \|C10.314.475
Synonyms:	Marchiafava Bignami Disease \|Marchiafava Bignami Syndrome \|Marchiafava-Bignami Syndrome
Slim Mappings:	Nervous system disease
Reference:	MedGen: D054319 MeSH: D054319 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants