ODCs

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2 OMIM references -
1 associated gene
10 signs/symptoms

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
14 signs/symptoms

Fibronectin glomerulopathy

Epidermolysis bullosa simplex with muscular dystrophy


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

Citations in the biomedical literature:

Fibronectin glomerulopathy		Epidermolysis bullosa simplex with muscular dystrophy
	Synonym(s): - GFND - Glomerulopathy with fibronectin deposits		Synonym(s): - EBS-MD - Limb girdle dystrophy with epidermolysis bullosa simplex

	Classification (Orphanet): - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic 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 recessive

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

Fibronectin glomerulopathy		Epidermolysis bullosa simplex with muscular dystrophy
	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 - Alopecia - Autosomal recessive inheritance - Muscle weakness / flaccidity - Myopathy - Ophthalmoplegia / ophthalmoparesis / oculomotor palsy - Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia - Thin / hypoplastic / hyperconvex fingernails - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment Frequent - Enamel anomaly - Follicular / erythematous / edematous papules / milium - Ptosis - Skin hypoplasia / aplasia / atrophy Occasional - Asthenia / fatigue / weakness - Myasthenia