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Progressive supranuclear palsy - corticobasal syndrome
1 associated gene
55 connected diseases
No signs/symptoms info
Disease Type of connection
Behavioral variant of frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Classical progressive supranuclear palsy
Progressive supranuclear palsy - parkinsonism
Progressive supranuclear palsy - progressive non fluent aphasia
Progressive supranuclear palsy - pure akinesia with gait freezing
Young adult-onset Parkinsonism
Amyotrophic lateral sclerosis
Early-onset autosomal dominant Alzheimer disease
Parkinsonian-pyramidal syndrome
Hyperlipidemia type 3
Lipoprotein glomerulopathy
Sea-blue histiocytosis
Cerebellar ataxia - hypogonadism
Congenital fibrosis of extraocular muscles
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
Cowden syndrome
Proteus syndrome
Coffin-Lowry syndrome
X-linked non-syndromic intellectual deficit
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
Catecholaminergic polymorphic ventricular tachycardia
Distal hereditary motor neuropathy type 7
Perry syndrome
Early infantile epileptic encephalopathy
Autosomal recessive centronuclear myopathy
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Chronic myeloid leukemia
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Autoimmune lymphoproliferative syndrome
Autosomal recessive systemic lupus erythematosus
Common variable immunodeficiency
Glycogen storage disease due to muscle phosphorylase kinase deficiency
Lissencephaly due to TUBA1A mutation
Familial advanced sleep-phase syndrome
Autoimmune lymphoproliferative syndrome with recurrent infections
Familial isolated dilated cardiomyopathy
Autosomal dominant hypohidrotic ectodermal dysplasia
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Hereditary spherocytosis
Partial chromosome Y deletion
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Familial Alzheimer-like prion disease
Fatal familial insomnia
Gerstmann-Straussler-Scheinker syndrome
Huntington disease-like 1
Inherited Creutzfeldt-Jakob disease
- PSP-corticobasal syndrome

Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references

Gene symbol UniProt reference OMIM reference
MAPT P10636157140
No signs/symptoms info available.