General Information of Disease (ID: DISIRPQ9)

Disease Name Familial Alzheimer-like prion disease
Disease Hierarchy
DISD715V: Hereditary neurological disease
DISOUMB0: Prion disease
DISIRPQ9: Familial Alzheimer-like prion disease
Disease Identifiers
MONDO ID
MONDO_0017233
UMLS CUI
C4303482
MedGen ID
929151
Orphanet ID
280397
SNOMED CT ID
721219005

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
PRNP TTY5F9C Definitive GermlineCausalMutation [1]
------------------------------------------------------------------------------------
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
PRNP OTE85L1Q Supportive Autosomal dominant [1]
------------------------------------------------------------------------------------

References

1 Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype. Ann Neurol. 2011 Apr;69(4):712-20. doi: 10.1002/ana.22264. Epub 2011 Mar 17.