MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
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frontotemporal degeneration with dementia (MONDO:0020137)
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frontotemporal neurodegeneration with movement disorder (MONDO:0017643)
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genetic neurodegenerative disease with dementia (MONDO:0021037)
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inherited tremor disorder (MONDO:0017663)
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corticobasal syndrome ()

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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:18696
Name:corticobasal syndrome
Definition:Corticobasal syndrome (CBS) is a rare neurodegenerative disease characterized by multifaceted motor system dysfunctions and cognitive defects such as asymmetric rigidity, bradykinesia, limb apraxia, and visuospatial dysfunction.
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