epidermolysis bullosa with congenital localized absence of skin and deformity of nails
MONDO:0007557Mondo
Findings
No curated finding names epidermolysis bullosa with congenital localized absence of skin and deformity of nails yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
6 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Abnormal blistering of the skinHPOHP:0008066
- Congenital localized absence of skinHPOHP:0007383
- Fragile skinHPOHP:0001030
- Nail dystrophyHPOHP:0008404
- Oral mucosal blistersHPOHP:0200097
- Sub-lamina densa cleavageHPOHP:0033803
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- COL7A1HGNC:2214
- Definitive · G2P · Autosomal dominant · 2019
- Strong · Genomics England PanelApp · Autosomal dominant · 2020
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
Where it sits
- A kind of