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:
expandnervous system disorder (MONDO:0005071)
..Starting node
..expandcentral nervous system disease ()

       Child 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 ()



 Sister Nodes: 
..expandautoimmune disease of the nervous system ()
..expandBalint syndrome ()
..expandBarre-Lieou syndrome ()
..expandcentral nervous system disease ()
..expandcerebral disease with cataract ()
..expandcomplex neurodevelopmental disorder ()
..expandcongenital nervous system disorder ()
..expandcranial nerve neuropathy ()
..expanddevelopmental disability ()
..expanddiplegia of upper limb ()
..expanddrug-induced akathisia ()
..expanddrug-induced dyskinesia ()
..expandgenetic nervous system disorder ()
..expandGerstmann syndrome ()
..expandidiopathic recurrent stupor ()
..expandinfectious disease of the nervous system ()
..expandinherited nervous system cancer-predisposing syndrome ()
..expandlocked-in syndrome ()
..expandmovement disorder ()
..expandneonatal brainstem dysfunction ()
..expandnervous system injury ()
..expandnervous system neoplasm ()
..expandneurocutaneous syndrome ()
..expandneuroendocrine disease ()
..expandneuronitis ()
..expandneurosarcoidosis ()
..expandneurovascular disease ()
..expandpalsy ()
..expandparaneoplastic neurologic syndrome ()
..expandperceptual disorders ()
..expandperineural cyst ()
..expandperipheral nervous system disease ()
..expandpersistent idiopathic facial pain ()
..expandprimary orthostatic hypotension ()
..expandradiculitis ()
..expandrare disease with malignant hyperthermia ()
..expandrare neuroinflammatory or neuroimmunological disease ()
..expandrare neurologic disease with psychiatric involvement ()
..expandrestless legs syndrome ()
..expandretinal disease ()
..expandsensory ganglionopathy ()
..expandsleep-wake disorder ()
..expandspecific learning disability ()
..expandspontaneous periodic hypothermia ()
..expandsymmetrical thalamic calcifications ()
..expandtoxic encephalopathy ()
..expandWallerian degeneration ()
..expandWorster-Drought syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:2602
Name:central nervous system disease
Definition:A disease involving the central nervous system.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:central nervous disease; central nervous system disease; central nervous system disease or disorder; central nervous system disorder; disease of central nervous system; disease or disorder of central nervous system; disorder of central nervous system; disorder of central nervous system
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes: ASCL1; BDNF; EDN3; GDNF; PHOX2B; RET;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal