ODCs

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1 OMIM reference -
1 associated gene
5 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 1

1 OMIM reference -
1 associated gene
9 signs/symptoms

Transient bullous dermolysis of the newborn

Pretibial dystrophic epidermolysis bullosa

Citations in the biomedical literature:

Transient bullous dermolysis of the newborn		Pretibial dystrophic epidermolysis bullosa
	Synonym(s): - DEB, bullous dermolysis of the newborn - DEB-BDN		Synonym(s): - DEB-Pt - Pretibial DEB

	Classification (Orphanet): - Rare developmental defect during embryogenesis - 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: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		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 - 1 MeSH reference: C536979		External references: 1 OMIM reference - No MeSH references


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

Transient bullous dermolysis of the newborn		Pretibial dystrophic epidermolysis bullosa
	Frequent - Irregular / patchy skin hypopigmentation - Nails anomalies - Oral mucosa disease / cheilitis - Thin skin		Very frequent - Abnormal fingernails - Abnormal toenails - Autosomal dominant inheritance Frequent - Abnormal scarring / cheloids / hypertrophic scars - Follicular / erythematous / edematous papules / milium - Pruritus / itching Occasional - Hyperkeratosis / ainhum / hyperkeratotic skin fissures - Lichen