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MCID: PRP089
MIFTS: 8
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Prp Systemic Amyloidosis
Categories:
Gastrointestinal diseases, Neuronal diseases, Rare diseases
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MalaCards integrated aliases for Prp Systemic Amyloidosis:
Name: Prp Systemic Amyloidosis
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:
ICD10:
33
Orphanet: 58
Rare neurological diseases
Rare gastroenterological diseases External Ids:
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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).
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Articles related to Prp Systemic Amyloidosis:(showing 1, show less)
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Genes related to Prp Systemic Amyloidosis (1 elite genes):(showing 1, show less) - Elite gene
- Cancer Census gene in COSMIC
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Search
GEO
for disease gene expression data for Prp Systemic Amyloidosis.
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