ODCs

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2 OMIM references -
1 associated gene
10 signs/symptoms

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
5 signs/symptoms

Fibronectin glomerulopathy

Transient bullous dermolysis of the newborn


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FN1	(0.85)	COL7A1

Citations in the biomedical literature:

Fibronectin glomerulopathy		Transient bullous dermolysis of the newborn
	Synonym(s): - GFND - Glomerulopathy with fibronectin deposits		Synonym(s): - DEB, bullous dermolysis of the newborn - DEB-BDN

	Classification (Orphanet): - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Diseases of the genitourinary system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	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 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C536979

Fibronectin glomerulopathy		Transient bullous dermolysis of the newborn
	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		Very frequent - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment Frequent - Irregular / patchy skin hypopigmentation - Nails anomalies - Oral mucosa disease / cheilitis - Thin skin