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1 OMIM reference -
2 associated genes
4 signs/symptoms
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
1 OMIM reference -
1 associated gene
6 signs/symptoms
Localized epidermolysis bullosa simplex
Naegeli-Franceschetti-Jadassohn syndrome

KRT14 KRT14
KRT5


COMMON
GENES
KRT14


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KRT5
(0.69)
KRT14



Citations in the biomedical literature:


Localized epidermolysis bullosa simplex
KRT14 KRT5
Naegeli-Franceschetti-Jadassohn syndrome



Localized epidermolysis bullosa simplex
Naegeli-Franceschetti-Jadassohn syndrome

Synonym(s):
- EBS-loc
- Epidermolysis bullosa simplex of palms and soles
- Epidermolysis bullosa simplex, Weber-Cockayne type

Synonym(s):
- NFJ syndrome
- Naegeli syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- 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: childhood
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant

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


COMMON
SIGNS
- Autosomal dominant inheritance


Localized epidermolysis bullosa simplex
Naegeli-Franceschetti-Jadassohn syndrome

Very frequent
- Ecchymoses
- Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment

Frequent
- Hyperhidrosis / increased sweating



Very frequent
- Dysplastic / thick / grooved fingernails
- Dysplastic / thick / grooved toenails
- Enamel anomaly
- Irregular / in bands / reticular skin hyperpigmentation
- Palmoplantar hyperkeratosis / keratoderma