epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive
MONDO:0014014Mondo
Findings
No curated finding names epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Childhood onset
HPO, annotations 2026-09-02
Features
4 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
- 3 of 3 reported patients
- Epidermal acanthosisHPOHP:0025092
- 1 of 1 reported patient
- Fragile skinHPOHP:0001030
- 3 of 3 reported patients
- HyperkeratosisHPOHP:0000962
- 1 of 1 reported patient
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.
- EXPH5HGNC:30578
- Strong · Genomics England PanelApp · Autosomal recessive · 2020
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2021
- Strong · G2P · Autosomal recessive · 2025
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Supportive · Orphanet · Autosomal recessive · 2021
Where it sits
- A kind of
Other names
2 names
Resolves to: epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive
- Also called
- EBS-AR exophilin 5epidermolysis bullosa simplex due to exophilin 5 deficiency