epidermolytic hyperkeratosis 2A, autosomal dominant
MONDO:0700248Mondo
Findings
No curated finding names epidermolytic hyperkeratosis 2A, autosomal dominant yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance · Autosomal recessive inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
8 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.
- Congenital nonbullous ichthyosiform erythrodermaHPOHP:0007479
- 2 of 2 reported patients
- ErythrodermaHPOHP:0001019
- 2 of 2 reported patients
- Generalized hyperkeratosisHPOHP:0005595
- 11 of 13 reported patients
- Palmoplantar keratodermaHPOHP:0000982
- 2 of 3 reported patients
- Cobblestone-like hyperkeratosisHPOHP:0031288
- 1 of 2 reported patients
- Abnormal blistering of the skinHPOHP:0008066
- 4 of 11 reported patients
- Palmoplantar hyperkeratosisHPOHP:0000972
- 2 of 10 reported patients
- HyperkeratosisHPOHP:0000962
- 1 of 8 reported patients
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.
- KRT10HGNC:6413
- Strong · Ambry Genetics · Autosomal dominant · 2024
- Strong · PanelApp Australia · Autosomal dominant · 2025