ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Progressive supranuclear palsy - corticobasal syndrome

Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation


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

Citations in the biomedical literature:

Progressive supranuclear palsy - corticobasal syndrome		Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
	Synonym(s): - PSP-CBS - PSP-corticobasal syndrome		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: 1-9 / 1 000 000 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: No OMIM references No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.