MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
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Parent Node:
expandnervous system disorder (MONDO:0005071)
..Starting node
..expandrare neurologic disease with psychiatric involvement ()

       Child Nodes:
........expand22q11.2 deletion syndrome ()
........expandAngelman syndrome ()
........expandchromosome 15q13.3 microdeletion syndrome ()
........expandearly-onset schizophrenia ()
........expandmyotonic dystrophy type 1 ()
........expandPrader-Willi syndrome ()
........expandPrader-Willi-like syndrome ()
........expandWilliams syndrome ()
........expandWilson 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:20016
Name:rare neurologic disease with psychiatric involvement
Definition:
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Synonyms:
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Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
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