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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Progressive supranuclear palsy - parkinsonism
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation

MAPT 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
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
TUBB3



Progressive supranuclear palsy - parkinsonism
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation

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

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.