MCID: SPR154
MIFTS: 10

Sporadic Human Prion Disease

Categories: Genetic diseases, Mental diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Sporadic Human Prion Disease

MalaCards integrated aliases for Sporadic Human Prion Disease:

Name: Sporadic Human Prion Disease 58
Idiopathic Human Prion Disease 58

Classifications:



External Ids:

Orphanet 58 ORPHA576356

Summaries for Sporadic Human Prion Disease

MalaCards based summary : Sporadic Human Prion Disease, also known as idiopathic human prion disease, is related to prion disease and creutzfeldt-jakob disease. An important gene associated with Sporadic Human Prion Disease is PRNP (Prion Protein). Affiliated tissues include brain.

Related Diseases for Sporadic Human Prion Disease

Diseases in the Prion Disease family:

Inherited Human Prion Disease Sporadic Human Prion Disease
Acquired Human Prion Disease

Diseases related to Sporadic Human Prion Disease via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 prion disease 10.3
2 creutzfeldt-jakob disease 10.1
3 variably protease-sensitive prionopathy 9.9

Symptoms & Phenotypes for Sporadic Human Prion Disease

Drugs & Therapeutics for Sporadic Human Prion Disease

Search Clinical Trials , NIH Clinical Center for Sporadic Human Prion Disease

Genetic Tests for Sporadic Human Prion Disease

Anatomical Context for Sporadic Human Prion Disease

MalaCards organs/tissues related to Sporadic Human Prion Disease:

40
Brain

Publications for Sporadic Human Prion Disease

Articles related to Sporadic Human Prion Disease:

# Title Authors PMID Year
1
Molecular Subtyping of PrPres in Human Sporadic CJD Brain Tissue. 61
28861800 2017
2
Real-Time Quaking-Induced Conversion for Diagnosis of Prion Disease. 61
28861798 2017
3
Transmission characteristics of variably protease-sensitive prionopathy. 61
25418590 2014
4
The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob disease. 61
25331173 2014
5
Molecular pathology, classification, and diagnosis of sporadic human prion disease variants. 61
22505361 2012
6
Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future. 61
21107851 2011
7
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain. 61
18234793 2008
8
Prion infections in Creutzfeldt-Jakob disease and its variants. 61
10219698 1999

Variations for Sporadic Human Prion Disease

Expression for Sporadic Human Prion Disease

Search GEO for disease gene expression data for Sporadic Human Prion Disease.

Pathways for Sporadic Human Prion Disease

GO Terms for Sporadic Human Prion Disease

Sources for Sporadic Human Prion Disease

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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