ODCs

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1 OMIM reference -
1 associated gene
5 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 2

1 associated gene
5 signs/symptoms

Transient bullous dermolysis of the newborn

Dystrophic epidermolysis bullosa, nails only

Citations in the biomedical literature:

Transient bullous dermolysis of the newborn		Dystrophic epidermolysis bullosa, nails only
	Synonym(s): - DEB, bullous dermolysis of the newborn - DEB-BDN		Synonym(s): - DEB-na - Nails-only DEB

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic 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 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: No OMIM references No MeSH references


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

Transient bullous dermolysis of the newborn		Dystrophic epidermolysis bullosa, nails only
	Frequent - Irregular / patchy skin hypopigmentation - Oral mucosa disease / cheilitis - Thin skin		Very frequent - Abnormal toenails - Autosomal dominant inheritance Occasional - Autosomal recessive inheritance