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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 OMIM references -
4 associated genes
No signs/symptoms info
Progressive supranuclear palsy - parkinsonism
Congenital fibrosis of extraocular muscles

MAPT KIF21A
PHOX2A
TUBB2B
TUBB3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MAPT
(0.84)
TUBB3



Citations in the biomedical literature:


Progressive supranuclear palsy - parkinsonism
MAPT
Congenital fibrosis of extraocular muscles
KIF21A PHOX2A TUBB2B TUBB3



Progressive supranuclear palsy - parkinsonism
Congenital fibrosis of extraocular muscles

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

Synonym(s):
- FEOM

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the eye and adnexa -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
6 OMIM references -
No MeSH references

No signs/symptoms info available.