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2 OMIM references -
1 associated gene
10 signs/symptoms
PROTEIN INTERACTIONS: 2
6 OMIM references -
7 associated genes
No signs/symptoms info
Fibronectin glomerulopathy
B-cell chronic lymphocytic leukemia

FN1 ARL11
ATM
CCND1
IGHG1
IGHV3-21
()
POT1
TP53


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FN1
FN1
(0.63)
(0.63)
IGHG1
IGHV3-21



Citations in the biomedical literature:


Fibronectin glomerulopathy
FN1
B-cell chronic lymphocytic leukemia
ARL11 ATM CCND1 IGHG1 IGHV3-21 POT1
TP53



Fibronectin glomerulopathy
B-cell chronic lymphocytic leukemia

Synonym(s):
- GFND
- Glomerulopathy with fibronectin deposits

Synonym(s):
- B-CLL
- B-cell chronic lymphoid leukemia
- Lymphoplasmacytic leukemia
- Lymphoplasmacytoid immunocytoma
- Small lymphocytic lymphoma

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic 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:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic

External references:
2 OMIM references -
No MeSH references
External references:
6 OMIM references -
1 MeSH reference: D015451

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


B-cell chronic lymphocytic leukemia

(no data available)