MCID: PRP089
MIFTS: 7

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 60
Chronic Diarrhea with Hereditary Sensory and Autonomic Neuropathy 60
Prion Protein Systemic Amyloidosis 60
Chronic Diarrhea with Hsan 60

Characteristics:

Orphanet epidemiological data:

60
prp systemic amyloidosis
Inheritance: Autosomal dominant; Prevalence: <1/1000000 (Worldwide); Age of onset: Adult; Age of death: adult,elderly;

Classifications:



External Ids:

ICD10 via Orphanet 35 G60.8
Orphanet 60 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

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
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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