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:
expandneurodegenerative disease with dementia (MONDO:0020136)
..Starting node
..expandhuman prion disease ()

       Child Nodes:
........expandinherited prion disease ()
........expandkuru ()
........expandvariably protease-sensitive prionopathy ()



 Sister Nodes: 
..expandamyotrophic lateral sclerosis-parkinsonism-dementia complex ()
..expandfrontotemporal degeneration with dementia ()
..expandgenetic neurodegenerative disease with dementia ()
..expandhuman prion disease ()
..expandprimary progressive aphasia ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:18926
Name:human prion disease
Definition:5%) include iatrogenic CJD and variant CJD (vCDJ).
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:transmissible spongiform encephalopathy; TSE
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal