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1 OMIM reference -
5 associated genes
5 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Generalized junctional epidermolysis bullosa, non-Herlitz type
Cobblestone lissencephaly without muscular or ocular involvement

COL17A1 LAMB1
ITGB4
LAMA3
LAMB3
LAMC2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LAMA3
(0.52)
LAMB1



Citations in the biomedical literature:


Generalized junctional epidermolysis bullosa, non-Herlitz type
COL17A1 ITGB4 LAMA3 LAMB3 LAMC2
Cobblestone lissencephaly without muscular or ocular involvement
LAMB1



Generalized junctional epidermolysis bullosa, non-Herlitz type
Cobblestone lissencephaly without muscular or ocular involvement

Synonym(s):
- GABEB
- Generalized atrophic benign epidermolysis bullosa
- JEB-nH gen
- Junctional epidermolysis bullosa generalisata mitis
- Junctional epidermolysis bullosa, Disentis type

Synonym(s):
- Cobblestone lissencephaly without muscular or eye involvement
- Lissencephaly type 2 without muscular or eye involvement
- Lissencephaly type 2 without muscular or ocular involvement

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare odontologic disease
- Rare skin disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal recessive
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:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

Generalized junctional epidermolysis bullosa, non-Herlitz type

Very frequent
- Nails anomalies
- Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment

Frequent
- Abnormal fingernails
- Abnormal toenails

Occasional
- Anomalies of teeth and dentition


Cobblestone lissencephaly without muscular or ocular involvement

(no data available)