MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandcentral nervous system disease (MONDO:0002602)
..Starting node
..expandbrain disease ()

       Child Nodes:
........expandakinetic mutism ()
........expandautoimmune encephalopathy with parasomnia and obstructive sleep apnea ()
........expandbasal ganglia disease ()
........expandbrain compression ()
........expandbrain edema ()
........expandbrain hypoxia - ischemia ()
........expandbrain inflammatory disease ()
........expandbrain injury ()
........expandbrain neoplasm ()
........expandcentral nervous system cyst (disease) ()
........expandcentral nervous system origin vertigo ()
........expandcerebellar disease ()
........expandcerebral cortex disease ()
........expandcerebral degeneration ()
........expandcerebral lipidosis with dementia ()
........expandcerebral malaria ()
........expandcerebral organic aciduria ()
........expandcerebral sarcoidosis ()
........expandcerebral sinovenous thrombosis ()
........expandcerebrovascular disorder ()
........expandcluster headache syndrome ()
........expandCOL4A1-related familial vascular leukoencephalopathy ()
........expandcolpocephaly ()
........expandcorpus callosum agenesis of blepharophimosis robin type ()
........expandcorpus callosum dysgenesis cleft spasm ()
........expandcorpus callosum dysgenesis hypopituitarism ()
........expandcorpus callosum dysgenesis X-linked recessive ()
........expanddelayed encephalopathy after acute carbon monoxide poisoning ()
........expanddiabetic encephalopathy ()
........expanddisorder of medulla oblongata ()
........expanddisorder of optic chiasm ()
........expandencephalomalacia ()
........expandencephalopathy due to defective mitochondrial and peroxisomal fission ()
........expandencephalopathy, acute, infection-induced ()
........expandencephalopathy, recurrent, of childhood ()
........expandepilepsy ()
........expandhepatic encephalopathy ()
........expandhydrocephalus ()
........expandintracranial hypertension ()
........expandintracranial hypotension ()
........expandkernicterus ()
........expandleukoencephalopathy, megalencephalic ()
........expandmeningoencephalocele ()
........expandmental disorder ()
........expandmidbrain disease ()
........expandmigraine disorder ()
........expandmultiple sclerosis ()
........expandnarcolepsy without cataplexy ()
........expandnarcolepsy-cataplexy syndrome ()
........expandneurometabolic disease ()
........expandobsolete hypoglycemic coma ()
........expandolfactory nerve disease ()
........expandpituitary gland disease ()
........expandprion disease ()
........expandprogressive bulbar palsy ()
........expandReye syndrome ()
........expandsubarachnoid hemorrhage (disease) ()
........expandthalamic disease ()
........expandtraumatic encephalopathy ()
........expandvisual pathway disease ()
........expandWernicke encephalopathy ()



 Sister Nodes: 
..expandautoimmune disease of central nervous system ()
..expandbrain disease ()
..expandcentral nervous system infectious disorder ()
..expandcentral nervous system neoplasm ()
..expandcentral nervous system vasculitis ()
..expandcentral retinal vein occlusion ()
..expandcerebrospinal fluid leak ()
..expandencephalomyelitis ()
..expandheadache disorder ()
..expandhemiplegia ()
..expandhigh pressure neurological syndrome ()
..expandneurodegenerative disease ()
..expandoptic nerve disease ()
..expandquadriplegia ()
..expandspinal cord disease ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:5560
Name:brain disease
Definition:A disease affecting the brain or part of the brain.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:brain disease; brain disease or disorder; disease of brain; disease or disorder of brain; disorder of brain; disorder of brain; encephalopathy
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal