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
  1. Hereditary palmoplantar keratoderma MONDO:0019272 80
  2. Ichthyosis MONDO:0019269 65
  3. Inherited epidermolysis bullosa MONDO:0019276 58
  4. Erythrokeratoderma MONDO:0019270 17
  5. Porokeratosis MONDO:0006602 12
  6. Keratosis pilaris atrophicans MONDO:0018855 LRP1 6
  7. Hereditary poikiloderma MONDO:0016382 4
  8. Neonatal inflammatory skin and bowel disease MONDO:0017411 2
  9. 13q12.3 microdeletion syndrome MONDO:0018474
  10. Darier disease MONDO:0007417 ATP2A2
  11. Hailey-Hailey disease MONDO:0008218 ATP2C1
  12. VPS13A-related neurodegenerative disease MONDO:0008695 VPS13A
  13. Absence of fingerprints-congenital milia syndrome MONDO:0007507 SMARCAD1
  14. Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome MONDO:0008696
  15. Aquagenic palmoplantar keratoderma MONDO:0044663
  16. Congenital erosive and vesicular dermatosis MONDO:0016503
  17. Hyperkeratosis lenticularis perstans MONDO:0007756
  18. Keratolytic winter erythema MONDO:0007854
  19. Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome MONDO:0011169 POMP
  20. Palmoplantar pustulosis MONDO:0015597
  21. Phrynoderma MONDO:0400004
  22. Psoriasis 14, pustular MONDO:0013626 IL36RN
  23. Punctate acrokeratoderma freckle-like pigmentation MONDO:0036918
  24. Seborrhea-like dermatitis with psoriasiform elements MONDO:0012446 ZNF750
  25. Zinc-responsive necrolytic acral erythema MONDO:0018586

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