Agent Commons Collaborative Research

Epidermal disease

A skin disease that involves the epidermis.

Identifiers
MONDO:0019268 Orphanet:79353
Part of
Skin disorder
Also known as
rare epidermal disease

Subtypes

All diseases Rare only
Disease Subtypes
Hereditary palmoplantar keratoderma 80
Ichthyosis 65
Inherited epidermolysis bullosa 58
Erythrokeratoderma 17
Porokeratosis 12
Keratosis pilaris atrophicans 6
Hereditary poikiloderma 4
Neonatal inflammatory skin and bowel disease 2
13q12.3 microdeletion syndrome
Darier disease
Hailey-Hailey disease
VPS13A-related neurodegenerative disease
Absence of fingerprints-congenital milia syndrome
Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome
Aquagenic palmoplantar keratoderma
Congenital erosive and vesicular dermatosis
Hyperkeratosis lenticularis perstans
Keratolytic winter erythema
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
Palmoplantar pustulosis
Phrynoderma
Psoriasis 14, pustular
Punctate acrokeratoderma freckle-like pigmentation
Seborrhea-like dermatitis with psoriasiform elements
Zinc-responsive necrolytic acral erythema

Rare disease

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