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2 OMIM references -
1 associated gene
10 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
1 OMIM reference -
1 associated gene
15 signs/symptoms
Fibronectin glomerulopathy
Caffey disease

FN1 COL1A1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FN1
(0.52)
COL1A1



Citations in the biomedical literature:


Fibronectin glomerulopathy
FN1
Caffey disease
COL1A1



Fibronectin glomerulopathy
Caffey disease

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

Synonym(s):
- Infantile cortical hyperostosis

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

Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -

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: unknown
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 -
No MeSH references


COMMON
SIGNS
- Autosomal dominant inheritance


Fibronectin glomerulopathy
Caffey disease

Very frequent
- 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
- Cellulitis / panniculitis / pseudocellulitis / inflammation of subcutaneous tissue
- Cortical anomaly / thick bone cortical layer

Frequent
- Bone tumefaction / swelling
- Fever / chilling
- Humour troubles / anxiety / depression / apathy / euphoria / irritability
- Hyperesthesia / allodynia / hyperalgia

Occasional
- Dense / thickened skull / calvarium / cranial / facial hyperostosis
- Facial structural asymmetry / facial hemiatrophy / facial hemihypertrophy
- Feeding disorder / dysphagia / swallowing / sucking disorder / esophageal dyskinesia
- Hypergammaglobulinemia
- Hyperleukocytosis / leukocytosis
- Proptosis / exophthalmos
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction
- Scoliosis