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Familial Alzheimer-like prion disease
1 associated gene
58 connected diseases
No signs/symptoms info
Disease Type of connection
Fatal familial insomnia
Gerstmann-Straussler-Scheinker syndrome
Huntington disease-like 1
Inherited Creutzfeldt-Jakob disease
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Athabaskan brainstem dysgenesis syndrome
Bosley-Salih-Alorainy syndrome
Dyskeratosis congenita
Familial exudative vitreoretinopathy
Hereditary North American Indian childhood cirrhosis
Huntington disease
Joubert syndrome
Joubert syndrome with ocular defect
Joubert syndrome with oculorenal defect
Joubert syndrome with renal defect
Juvenile Huntington disease
Ligneous conjunctivitis
Reducing body myopathy
X-linked Emery-Dreifuss muscular dystrophy
X-linked myopathy with postural muscle atrophy
Autosomal dominant spastic paraplegia type 13
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Early infantile epileptic encephalopathy
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
Autosomal dominant microcephaly
Congenital lethal myopathy, Compton-North type
Hirschsprung disease
Hydrocephalus with stenosis of aqueduct of Sylvius
Hyperlipidemia type 3
Idiopathic ventricular fibrillation, not Brugada type
Lipoprotein glomerulopathy
MASA syndrome
Sea-blue histiocytosis
X-linked complicated corpus callosum dysgenesis
X-linked complicated spastic paraplegia type 1
Zlotogora-Ogur syndrome
Behavioral variant of frontotemporal dementia
Classical progressive supranuclear palsy
Familial partial lipodystrophy associated with PPARG mutations
Giant cell glioblastoma
Progressive non-fluent aphasia
Progressive supranuclear palsy - corticobasal syndrome
Progressive supranuclear palsy - parkinsonism
Progressive supranuclear palsy - progressive non fluent aphasia
Progressive supranuclear palsy - pure akinesia with gait freezing
Semantic dementia
(no synonyms)

Classification (Orphanet):
- Rare neurologic disease

Classification (ICD10):
- Certain infectious and parasitic diseases -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references

Gene symbol UniProt reference OMIM reference
PRNP P04156176640
No signs/symptoms info available.