MCID: PRP089
MIFTS: 8

Prp Systemic Amyloidosis

Categories: Gastrointestinal diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Prp Systemic Amyloidosis

MalaCards integrated aliases for Prp Systemic Amyloidosis:

Name: Prp Systemic Amyloidosis 58
Chronic Diarrhea with Hereditary Sensory and Autonomic Neuropathy 58
Prion Protein Systemic Amyloidosis 58
Chronic Diarrhea with Hsan 58

Characteristics:

Orphanet epidemiological data:

58
prp systemic amyloidosis
Inheritance: Autosomal dominant; Prevalence: <1/1000000 (Worldwide); Age of onset: Adult; Age of death: adult,elderly;

Classifications:

Orphanet: 58  
Rare neurological diseases
Rare gastroenterological diseases


External Ids:

ICD10 via Orphanet 33 G60.8
Orphanet 58 ORPHA397606

Summaries for Prp Systemic Amyloidosis

MalaCards based summary : Prp Systemic Amyloidosis, is also known as chronic diarrhea with hereditary sensory and autonomic neuropathy. An important gene associated with Prp Systemic Amyloidosis is PRNP (Prion Protein).

Related Diseases for Prp Systemic Amyloidosis

Symptoms & Phenotypes for Prp Systemic Amyloidosis

Drugs & Therapeutics for Prp Systemic Amyloidosis

Search Clinical Trials , NIH Clinical Center for Prp Systemic Amyloidosis

Genetic Tests for Prp Systemic Amyloidosis

Anatomical Context for Prp Systemic Amyloidosis

Publications for Prp Systemic Amyloidosis

Articles related to Prp Systemic Amyloidosis:

# Title Authors PMID Year
1
A new prion disease: relationship with central and peripheral amyloidoses. 61
25623792 2015

Variations for Prp Systemic Amyloidosis

Expression for Prp Systemic Amyloidosis

Search GEO for disease gene expression data for Prp Systemic Amyloidosis.

Pathways for Prp Systemic Amyloidosis

GO Terms for Prp Systemic Amyloidosis

Sources for Prp Systemic Amyloidosis

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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