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Fibronectin glomerulopathy

2 OMIM references -
1 associated gene
10 signs/symptoms

PROTEIN INTERACTIONS: 2

Hemoglobin H disease

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

Fibronectin glomerulopathy

Hemoglobin H disease

FN1	(UniProt - OMIM)		HBA1	(UniProt - OMIM)
			HBA2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FN1 FN1	(0.63) (0.63)	HBA1 HBA2

Citations in the biomedical literature:

Fibronectin glomerulopathy		Hemoglobin H disease
	Synonym(s): - GFND - Glomerulopathy with fibronectin deposits		Synonym(s): - Alpha-thalassemia intermedia - HbH disease

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

	Classification (ICD10): - Diseases of the genitourinary system -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	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: 1-9 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive

	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
Hemoglobin H disease
(no data available)