ODCs

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4 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Combined pituitary hormone deficiencies, genetic forms

Spinocerebellar ataxia type 1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	OTX2	(0.73)	ATXN1

Citations in the biomedical literature:

Combined pituitary hormone deficiencies, genetic forms		Spinocerebellar ataxia type 1
	Synonym(s): - Familial congenital hypopituitarism - Multiple pituitary hormone deficiencies, genetic forms		Synonym(s): - SCA1

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.