ODCs

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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

ANE syndrome

Spinocerebellar ataxia type 36


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RBM28	(0.63)	NOP56

Citations in the biomedical literature:

ANE syndrome		Spinocerebellar ataxia type 36
	Synonym(s): - Alopecia - progressive neurological defect - endocrinopathy		Synonym(s): - SCA36

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare infertility - Rare neurologic disease - Rare skin disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood 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.