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2 OMIM references -
2 associated genes
10 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 2
1 OMIM reference -
1 associated gene
4 signs/symptoms
Epidermolytic ichthyosis
Epidermolysis bullosa simplex with circinate migratory erythema

KRT1 KRT5
KRT10


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KRT1
(0.52)
KRT5



Citations in the biomedical literature:


Epidermolytic ichthyosis
KRT1 KRT10
Epidermolysis bullosa simplex with circinate migratory erythema
KRT5



Epidermolytic ichthyosis
Epidermolysis bullosa simplex with circinate migratory erythema

Synonym(s):
- BCIE
- Bullous congenital ichthyosiform erythroderma
- Bullous congenital ichthyosiform erythroderma of Brock
- Bullous ichthyosis
- EHK
- EI
- Epidermolytic hyperkeratosis

Synonym(s):
- EBS-migr

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

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: neonatal/infancy
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
- Erythema / erythematous lesions / erythroderma / polymorphous erythema
- Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment


Epidermolytic ichthyosis
Epidermolysis bullosa simplex with circinate migratory erythema

Very frequent
- Autosomal dominant inheritance
- Hyperkeratosis / ainhum / hyperkeratotic skin fissures
- Ichthyosis / ichthyosiform dermatitis
- Weight loss / loss of appetite / break in weight curve / general health alteration

Frequent
- Pigmented naevi / naevus pigmentosus / lentigo

Occasional
- Chronic skin infection / ulcerations / ulcers / cancrum
- Follicular / conjunctival hamartomas
- Palmoplantar hyperkeratosis / keratoderma


Very frequent
- Abnormal pigmentary skin changes / skin pigmentation anomalies
- Cutaneous rash