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Gardner syndrome

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

PROTEIN INTERACTIONS: 1

Autosomal recessive ataxia, Beauce type

1 OMIM reference -
1 associated gene
1 sign/symptom

Gardner syndrome

Autosomal recessive ataxia, Beauce type

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	APC	(0.63)	SYNE1

Citations in the biomedical literature:

Gardner syndrome		Autosomal recessive ataxia, Beauce type
	Synonym(s): (no synonyms)		Synonym(s): - ARCA1 - Autosomal recessive cerebellar ataxia type 1 - SCAR8

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

	Classification (ICD10): - Neoplasms -		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: no data available Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - 1 MeSH reference: D005736		External references: 1 OMIM reference - No MeSH references

Autosomal recessive ataxia, Beauce type
	Very frequent - Ataxia / incoordination / trouble of the equilibrium
Gardner syndrome
(no data available)