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spongiform encephalopathy with neuropsychiatric features
Disease Summary
Associated Targets (2)
Tchem
1
Tbio
1
Uniprot Description Autosomal dominant presenile dementia with a rapidly progressive and protracted clinical course. The dementia was characterized clinically by frontotemporal features, including early personality changes. Some patients had memory loss, several showed aggressiveness, hyperorality and verbal stereotypy, others had parkinsonian symptoms.
Mondo Term and Equivalent IDs
MONDO:0011703: spongiform encephalopathy with neuropsychiatric features
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
MESH:C564678
OMIM:606688
UMLS:C1847650
MONDO:0011703
High level summary of knowledge for a disease, including descriptions and datasource references.