epidermolytic hyperkeratosis 2B, autosomal recessive
MONDO:0700245Mondo
Findings
No curated finding names epidermolytic hyperkeratosis 2B, 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
- Congenital onset
HPO, annotations 2026-09-02
Features
11 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.
- Epidermal acanthosisHPOHP:0025092
- 4 of 4 reported patients
- ErythrodermaHPOHP:0001019
- 3 of 3 reported patients
- Generalized hyperkeratosisHPOHP:0005595
- 2 of 2 reported patients
- HypergranulosisHPOHP:0025114
- 2 of 2 reported patients
- Keratinocyte vacuolizationHPOHP:0034703
- 2 of 2 reported patients
- OrthokeratosisHPOHP:0040162
- 1 of 1 reported patient
- Congenital nonbullous ichthyosiform erythrodermaHPOHP:0007479
- 3 of 4 reported patients
- Abnormal blistering of the skinHPOHP:0008066
- 2 of 4 reported patients
- Cobblestone-like hyperkeratosisHPOHP:0031288
- 1 of 2 reported patients
- Hypernatremic dehydrationHPOHP:0004906
- 1 of 4 reported patients
- Palmoplantar keratodermaHPOHP:0000982
- 0 of 4 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 · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Ambry Genetics · Autosomal recessive · 2024