ODCs

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1 OMIM reference -
1 associated gene
16 signs/symptoms

PROTEIN INTERACTIONS: 1

4 OMIM references -
5 associated genes
No signs/symptoms info

Generalized dominant dystrophic epidermolysis bullosa

Osteogenesis imperfecta type 2


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL7A1	(0.75)	COL1A1

Citations in the biomedical literature:

Generalized dominant dystrophic epidermolysis bullosa		Osteogenesis imperfecta type 2
	Synonym(s): - Autosomal dominant dystrophic epidermolysis bullosa, Pasini and Cockayne-Touraine types - DDEB, Pasini and Cockayne-Touraine types - DDEB, generalized - DDEB-gen		Synonym(s): - Lethal osteogenesis imperfecta - OI type 2

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic 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: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 4 OMIM references - No MeSH references

Generalized dominant dystrophic epidermolysis bullosa
	Very frequent - Abnormal fingernails - Abnormal toenails - Autosomal dominant inheritance - Oral mucosa disease / cheilitis - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment 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
Osteogenesis imperfecta type 2
(no data available)