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:
expandhead disease (MONDO:0005042)
Parent Node:
expandnervous system disorder (MONDO:0005071)
..Starting node
..expandcranial nerve neuropathy ()

       Child Nodes:
........expandabducens nerve disease ()
........expandaccessory nerve disease ()
........expandcranial nerve neoplasm ()
........expandcranial nerve palsy ()
........expandcranial neuralgia ()
........expandfacial nerve disease ()
........expandglossopharyngeal nerve disease ()
........expandhypoglossal nerve disease ()
........expandjaw-winking syndrome ()
........expandocular motility disease ()
........expandolfactory nerve disease ()
........expandoptic nerve disease ()
........expandpseudobulbar palsy ()
........expandthird cranial nerve disease ()
........expandtrigeminal nerve disease ()
........expandtrochlear nerve disease ()
........expandvestibulocochlear nerve 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:3569
Name:cranial nerve neuropathy
Definition:A neoplastic or non-neoplastic disorder that affects one of the cranial nerves.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:cranial nerve disease; cranial nerve disease; cranial nerve disorder; cranial nerve disorder; cranial neuron projection bundle disease; cranial neuron projection bundle disease or disorder; cranial neuropathy; disease of cranial neuron projection bundle; disease or disorder of cranial neuron project
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes: TOR1A;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal