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MCID: FML202
MIFTS: 10
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Familial Alzheimer-Like Prion Disease
Categories:
Genetic diseases, Neuronal diseases, Rare diseases
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MalaCards integrated aliases for Familial Alzheimer-Like Prion Disease:
Name: Familial Alzheimer-Like Prion Disease
58
Characteristics:Orphanet epidemiological data:58
familial alzheimer-like prion disease
Inheritance: Autosomal dominant; Prevalence: <1/1000000 (Worldwide); Age of onset: Adult; Classifications:
ICD10:
33
Orphanet: 58
Rare neurological diseases External Ids:
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MalaCards based summary :
Familial Alzheimer-Like Prion Disease An important gene associated with Familial Alzheimer-Like Prion Disease is PRNP (Prion Protein). Related phenotypes are sleep disturbance and emotional lability
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Human phenotypes related to Familial Alzheimer-Like Prion Disease:58 31 (show all 12)
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Search
GEO
for disease gene expression data for Familial Alzheimer-Like Prion Disease.
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