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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
5 associated genes
No signs/symptoms info
Progressive supranuclear palsy - parkinsonism
Hereditary spherocytosis

MAPT ANK1
EPB42
SLC4A1
SPTA1
SPTB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MAPT
(0.52)
SPTB



Citations in the biomedical literature:


Progressive supranuclear palsy - parkinsonism
MAPT
Hereditary spherocytosis
ANK1 EPB42 SLC4A1 SPTA1 SPTB



Progressive supranuclear palsy - parkinsonism
Hereditary spherocytosis

Synonym(s):
- PSP-p
- PSP-parkinsonism

Synonym(s):
- Minkowski-Chauffard disease

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
4 OMIM references -
2 MeSH references: C536356 / D013103

No signs/symptoms info available.