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1 OMIM reference -
1 associated gene
8 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
2 OMIM references -
1 associated gene
10 signs/symptoms
Superficial epidermolytic ichthyosis
Fibronectin glomerulopathy

KRT2 FN1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KRT2
(0.72)
FN1



Citations in the biomedical literature:


Superficial epidermolytic ichthyosis
KRT2
Fibronectin glomerulopathy
FN1



Superficial epidermolytic ichthyosis
Fibronectin glomerulopathy

Synonym(s):
- Ichthyosis bullosa of Siemens
- SEI

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

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

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: no data available
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D053560
External references:
2 OMIM references -
No MeSH references


COMMON
SIGNS
- Autosomal dominant inheritance


Superficial epidermolytic ichthyosis
Fibronectin glomerulopathy

Very frequent
- Cutaneous edema
- Ichthyosis / ichthyosiform dermatitis
- Palmoplantar hyperkeratosis / keratoderma
- Positive Nikolski's sign / achantolysis
- Thin skin
- Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment

Occasional
- Erythema / erythematous lesions / erythroderma / polymorphous erythema


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