Skin pigmentation disorder

Part of

Sub-types of Skin pigmentation disorder

• Hyperpigmentation of the skin 17 trials · 31 incl. sub-types
  24 sub-types

  • Legius syndrome 5 trials
  • Dowling-Degos disease 0 trials · 4 incl. sub-types Sub-types →
  • Schwannomatosis 3 trials Sub-types →
  • Dyschromatosis symmetrica hereditaria 1 trial
  • Dyschromatosis universalis hereditaria 1 trial Sub-types →
  • H syndrome 0 trials
  • Naegeli-Franceschetti-Jadassohn syndrome 0 trials
  • Acromelanosis 0 trials
  • Cafe au lait spots, multiple 0 trials
  • Dermatopathia pigmentosa reticularis 0 trials
  • Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome 0 trials
  • Familial generalized lentiginosis 0 trials
  • Familial progressive hyperpigmentation 0 trials Sub-types →
  • Gastrocutaneous syndrome 0 trials
  • Hyperkeratosis-hyperpigmentation syndrome 0 trials
  • Hyperpigmentation, progressive cribriform and zosteriform 0 trials
  • Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome 0 trials
  • Linear and whorled nevoid hypermelanosis 0 trials
  • Mosaic Legius syndrome 0 trials
  • Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome 0 trials
  • Osteopathia striata-pigmentary dermopathy-white forelock syndrome 0 trials
  • Phakomatosis pigmentovascularis 0 trials Sub-types →
  • Reticulate acropigmentation of Kitamura 0 trials
  • Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome 0 trials
• Hypopigmentation of the skin 2 trials · 21 incl. sub-types
  10 sub-types

  • Syndromic oculocutaneous albinism 0 trials · 12 incl. sub-types Sub-types →
  • Oculocutaneous albinism 4 trials Sub-types →
  • Piebaldism 4 trials
  • Tietz syndrome 1 trial
  • Ito hypomelanosis 0 trials
  • Albinism-hearing loss syndrome 0 trials
  • Deaf blind hypopigmentation syndrome, Yemenite type 0 trials
  • Deafness, congenital, with total albinism 0 trials
  • Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies 0 trials
  • Piebald trait-neurologic defects syndrome 0 trials
• Reticulate pigment disorder 0 trials · 5 incl. sub-types
  3 sub-types

  • Dowling-Degos disease 0 trials · 4 incl. sub-types Sub-types →
  • Dyschromatosis symmetrica hereditaria 1 trial
  • Reticulate acropigmentation of Kitamura 0 trials
• Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome 0 trials