Agent Commons Collaborative Research

Hyperpigmentation of the skin

Identifiers
MONDO:0019289 Orphanet:79375
Part of
Skin pigmentation disorder

Subtypes

All diseases Rare only
Disease Subtypes
  1. Schwannomatosis MONDO:0008075 5
  2. Dowling-Degos disease MONDO:0008371 4
  3. Dyschromatosis universalis hereditaria MONDO:0000736 3
  4. Phakomatosis pigmentovascularis MONDO:0017318 3
  5. Familial progressive hyperpigmentation MONDO:0013648 2
  6. H syndrome MONDO:0011273 SLC29A3
  7. Legius syndrome MONDO:0012669 SPRED1
  8. Naegeli-Franceschetti-Jadassohn syndrome MONDO:0008059 KRT14
  9. Acromelanosis MONDO:0018311
  10. Cafe au lait spots, multiple MONDO:0007245
  11. Dermatopathia pigmentosa reticularis MONDO:0007445 KRT14
  12. Dyschromatosis symmetrica hereditaria MONDO:0007483
  13. Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome MONDO:0007588
  14. Familial generalized lentiginosis MONDO:0007891
  15. Gastrocutaneous syndrome MONDO:0007651
  16. Hyperkeratosis-hyperpigmentation syndrome MONDO:0007757
  17. Hyperpigmentation, progressive cribriform and zosteriform MONDO:0800357
  18. Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome MONDO:0016213
  19. Linear and whorled nevoid hypermelanosis MONDO:0013688
  20. Mosaic Legius syndrome MONDO:0859007
  21. Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome MONDO:0014460 GRHL2
  22. Osteopathia striata-pigmentary dermopathy-white forelock syndrome MONDO:0017197
  23. Reticulate acropigmentation of Kitamura MONDO:0014234 ADAM10
  24. Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome MONDO:0014886 PUS3

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