ODCs

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1 associated gene
30 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 4

1 OMIM reference -
1 associated gene
9 signs/symptoms

Recessive dystrophic epidermolysis bullosa-generalized other

Dystrophic epidermolysis bullosa pruriginosa

Citations in the biomedical literature:

Recessive dystrophic epidermolysis bullosa-generalized other		Dystrophic epidermolysis bullosa pruriginosa
	Synonym(s): - Autosomal recessive dystrophic epidermolysis bullosa generalisata mitis - Autosomal recessive dystrophic epidermolysis bullosa, generalized other - Generalized mitis RDEB - RDEB generalisata mitis - RDEB, non-Hallopeau-Siemens type - RDEB-O - RDEB-generalized other - Recessive dystrophic epidermolysis bullosa, non-Hallopeau-Siemens type		Synonym(s): - DEB, pruriginosa - DEB-Pr - Pruriginous dystrophic epidermolysis bullosa

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - 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: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

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


COMMON SIGNS	- Abnormal scarring / cheloids / hypertrophic scars - Autosomal recessive inheritance - Follicular / erythematous / edematous papules / milium - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment

Recessive dystrophic epidermolysis bullosa-generalized other		Dystrophic epidermolysis bullosa pruriginosa
	Very frequent - Abnormal fingernails - Abnormal toenails Frequent - Ankyloglossia / lingual synechiae - Anus / rectum anomalies - Constipation - Enanthema / aphtosa / aphta / leukoplakia - Feeding disorder / dysphagia / swallowing / sucking disorder / esophageal dyskinesia - Microstomia / little mouth - Multiple caries - Skin / cutaneous neoplasm / tumor / carcinoma / cancer (excluding melanoma) - Tracheo-esophageal fistula / esophageal atresia / stenosis Occasional - Alopecia - Anaemia - Anomalies of eyelids, eyelashes and lacrimal system - Corneal ulceration / perforation - Cryptophthalmia / ankyloblepharon / synblepharon - Ectropion / entropion / eyelid eversion - Failure to thrive / difficulties for feeding in infancy / growth delay - Hair and scalp anomalies - Late puberty / hypogonadism / hypogenitalism - Musculo-tendinous retractions - Osteoporosis / osteopenia / demineralisation / osteomalacia / rickets - Skin hypoplasia / aplasia / atrophy - Syndactyly of fingers / interdigital palm - Syndactyly of toes - Visual loss / blindness / amblyopia		Very frequent - Autosomal dominant inheritance - Pruritus / itching - Thin skin Frequent - Lichen - Nails anomalies