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Fibronectin glomerulopathy

2 OMIM references -
1 associated gene
10 signs/symptoms

PROTEIN INTERACTIONS: 1

Fetal and neonatal alloimmune thrombocytopenia

6 associated genes
No signs/symptoms info

Fibronectin glomerulopathy

Fetal and neonatal alloimmune thrombocytopenia

FN1	(UniProt - OMIM)		CD109	(UniProt - OMIM)
			GP1BA	(UniProt - OMIM)
			GP1BB	(UniProt - OMIM)
			ITGA2	(UniProt - OMIM)
			ITGA2B	(UniProt - OMIM)
			ITGB3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FN1	(0.62)	ITGB3

Citations in the biomedical literature:

Fibronectin glomerulopathy		Fetal and neonatal alloimmune thrombocytopenia
	Synonym(s): - GFND - Glomerulopathy with fibronectin deposits		Synonym(s): - NAIT

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

	Classification (ICD10): - Diseases of the genitourinary system -		Classification (ICD10): - Certain conditions originating in the perinatal period -

	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: No 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
Fetal and neonatal alloimmune thrombocytopenia
(no data available)