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Fibronectin glomerulopathy
2 OMIM references -
1 associated gene
10 signs/symptoms
PROTEIN INTERACTIONS: 3
Translocation renal cell carcinoma
1 OMIM reference -
7 associated genes
No signs/symptoms info
Fibronectin glomerulopathy
Translocation renal cell carcinoma

FN1
(UniProt - OMIM)
 ASPSCR1
(UniProt - OMIM)
CLTC
(UniProt - OMIM)
NONO
(UniProt - OMIM)
PRCC
(UniProt - OMIM)
SFPQ
(UniProt - OMIM)
TFE3
(UniProt - OMIM)
TFEB
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FN1
FN1
FN1
(0.72)
(0.63)
(0.63)
CLTC
NONO
SFPQ


Citations in the biomedical literature:


Fibronectin glomerulopathy
FN1
Translocation renal cell carcinoma
ASPSCR1 CLTC NONO PRCC SFPQ TFE3
TFEB



Fibronectin glomerulopathy
Translocation renal cell carcinoma

Synonym(s):
- GFND
- Glomerulopathy with fibronectin deposits
Synonym(s):
- Carcinoma associated with MITF/TFE translocation
- Translocation carcinoma
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare oncologic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
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


Translocation renal cell carcinoma

(no data available)