ODCs

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1 OMIM reference -
1 associated gene
3 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 2

1 associated gene
5 signs/symptoms

Junctional epidermolysis bullosa inversa

Dystrophic epidermolysis bullosa, nails only


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LAMC2	(0.76)	COL7A1

Citations in the biomedical literature:

Junctional epidermolysis bullosa inversa		Dystrophic epidermolysis bullosa, nails only
	Synonym(s): - EBJ-I - Inverse JEB - JEB-I		Synonym(s): - DEB-na - Nails-only DEB

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare odontologic 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 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - 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 dominant

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


COMMON SIGNS	- Autosomal recessive inheritance - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment

Junctional epidermolysis bullosa inversa		Dystrophic epidermolysis bullosa, nails only
	Frequent - Abnormal fingernails		Very frequent - Abnormal toenails - Autosomal dominant inheritance - Nails anomalies