epidermal disease
MONDO:0019268Mondo
Findings
No curated finding names epidermal disease yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A skin disease that involves the epidermis.
Definition from the Mondo Disease Ontology (MONDO:0019268), read 2026-09-29. CC BY 4.0.
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.
- KLF4HGNC:6348
- Moderate · Ambry Genetics · Autosomal dominant · 2025
Where it sits
- A kind of
- Narrower terms (25)
- 13q12.3 microdeletion syndrome
- absence of fingerprints-congenital milia syndrome
- acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome
- aquagenic palmoplantar keratoderma
- congenital erosive and vesicular dermatosis
- Darier disease
- erythrokeratoderma
- Hailey-Hailey disease
- hereditary palmoplantar keratoderma
- hereditary poikiloderma
- hyperkeratosis lenticularis perstans
- ichthyosis
- inherited epidermolysis bullosa
- keratolytic winter erythema
- keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
- keratosis pilaris atrophicans
- neonatal inflammatory skin and bowel disease
- palmoplantar pustulosis
- phrynoderma
- porokeratosis
Other names
1 name
Resolves to: epidermal disease
- Also called
- rare epidermal disease