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Spinocerebellar ataxia type 26

1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

Fibronectin glomerulopathy

2 OMIM references -
1 associated gene
10 signs/symptoms

Spinocerebellar ataxia type 26

Fibronectin glomerulopathy

EEF2	(UniProt - OMIM)		FN1	(UniProt - OMIM)
SCA26


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EEF2 SCA26	(0.72) (0.63)	FN1 FN1

Citations in the biomedical literature:

Spinocerebellar ataxia type 26		Fibronectin glomerulopathy
	Synonym(s): - SCA26		Synonym(s): - GFND - Glomerulopathy with fibronectin deposits

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare renal disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the genitourinary system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C537203		External references: 2 OMIM references - No MeSH references

Fibronectin glomerulopathy
	Very frequent - Autosomal dominant inheritance - Chronic arterial hypertension - Edema of the legs / lower limbs - Functional anomalies of the kidney and the urinary tract - Hematuria / microhematuria - Nephrotic syndrome - Proteinuria - Renal failure - Renal glomerular defect / glomerulopathy Occasional - Intracranial / cerebral / meningeal hemorrhage
Spinocerebellar ataxia type 26
(no data available)