MCID: PRP089
MIFTS: 7

Prp Systemic Amyloidosis

Categories: Neuronal diseases, Gastrointestinal diseases, Rare diseases

Aliases & Classifications for Prp Systemic Amyloidosis

MalaCards integrated aliases for Prp Systemic Amyloidosis:

Name: Prp Systemic Amyloidosis 59
Chronic Diarrhea with Hereditary Sensory and Autonomic Neuropathy 59
Prion Protein Systemic Amyloidosis 59
Chronic Diarrhea with Hsan 59

Characteristics:

Orphanet epidemiological data:

59
prp systemic amyloidosis
Inheritance: Autosomal dominant; Prevalence: <1/1000000 (Worldwide); Age of onset: Adult; Age of death: adult,elderly;

Classifications:



External Ids:

Orphanet 59 ORPHA397606
ICD10 via Orphanet 34 G60.8

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 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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