ODCs

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1 OMIM reference -
1 associated gene
3 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 2

1 OMIM reference -
1 associated gene
16 signs/symptoms

Junctional epidermolysis bullosa inversa

Generalized dominant dystrophic epidermolysis bullosa


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

Citations in the biomedical literature:

Junctional epidermolysis bullosa inversa		Generalized dominant dystrophic epidermolysis bullosa
	Synonym(s): - EBJ-I - Inverse JEB - JEB-I		Synonym(s): - Autosomal dominant dystrophic epidermolysis bullosa, Pasini and Cockayne-Touraine types - DDEB, Pasini and Cockayne-Touraine types - DDEB, generalized - DDEB-gen

	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 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: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

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


COMMON SIGNS	- Abnormal fingernails - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment

Junctional epidermolysis bullosa inversa		Generalized dominant dystrophic epidermolysis bullosa
	Very frequent - Autosomal recessive inheritance		Very frequent - Abnormal toenails - Autosomal dominant inheritance - Oral mucosa disease / cheilitis Frequent - Abnormal scarring / cheloids / hypertrophic scars - Irregular / patchy skin hypopigmentation - Multiple caries - Skin hypoplasia / aplasia / atrophy Occasional - Anaemia - Corneal ulceration / perforation - Feeding disorder / dysphagia / swallowing / sucking disorder / esophageal dyskinesia - Follicular / erythematous / edematous papules / milium - Pollakiuria / polyuria / dysuria / anuria / acute urine retention / oliguria - Tracheo-esophageal fistula / esophageal atresia / stenosis - Urethral anomalies / stenosis / posterior urethral valves / megalocystis