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Acral dystrophic epidermolysis bullosa

1 associated gene
6 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 4

Dystrophic epidermolysis bullosa, nails only

1 associated gene
5 signs/symptoms

Acral dystrophic epidermolysis bullosa

Dystrophic epidermolysis bullosa, nails only

(UniProt - OMIM)

(UniProt - OMIM)


COMMON GENES	COL7A1

Citations in the biomedical literature:

Acral dystrophic epidermolysis bullosa		Dystrophic epidermolysis bullosa, nails only
	Synonym(s): - DEB, acral - DEB-ac		Synonym(s): - DEB-na - Nails-only DEB

	Classification (Orphanet): - 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: No OMIM references No MeSH references		External references: No OMIM references No MeSH references


COMMON SIGNS	- Autosomal dominant inheritance - Autosomal recessive inheritance - Nails anomalies - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment

Acral dystrophic epidermolysis bullosa		Dystrophic epidermolysis bullosa, nails only
	Very frequent - Follicular / erythematous / edematous papules / milium - Skin hypoplasia / aplasia / atrophy		Very frequent - Abnormal toenails