Skin pigment abnormality

Subtypes
Pigmented nevus
May Be Caused by
Acrodysostosis
Acrogeria
Addison disease
ADULT syndrome
Alkaptonuria
Ataxia-telangiectasia
Bannayan-Riley-Ruvalcaba syndrome
Bloom syndrome
Brachmann-de Lange syndrome
Carbon baby
Carney complex
Chédiak-Higashi syndrome
Chondrodysplasia punctata Conradi-Hünermann type
Chondrodysplasia punctata rhizomelic type
Chondrodysplasia punctata X-linked dominant type
Chromosomal mosaicism
Cleidocranial dysostosis
Clouston syndrome
Copper deficiency
Cronkhite-Canada syndrome
Cross syndrome
Cutis tricolor
De Sanctis-Cacchione syndrome
Dyskeratosis congenita
EEC syndrome
Epidermal nevus syndrome
Fanconi anemia
Farber syndrome
Felty syndrome
Gastrocutaneous syndrome
Gaucher disease
Goeminne syndrome
Goltz syndrome
Gorlin syndrome
Graft-versus-host disease
Griscelli syndrome
Hay-Wells syndrome
Hemihypertrophy
Hemochromatosis
Hermansky-Pudlak syndrome
Homocystinuria
Hyperphosphatasemia
Hypohidrotic ectodermal dysplasia
Hypomelanosis of Ito
Incontinentia pigmenti
Infantile digital fibromatosis-pigmentary defects syndrome
Jaffe-Campanacci syndrome
Klein-Waardenburg syndrome
Klippel-Trénaunay-Weber syndrome
Kuskokwim syndrome
LAMB syndrome
Lelis syndrome
LEOPARD syndrome
Lipodystrophy
Macrocephaly-cutis marmorata telangiectasia syndrome
Maffucci syndrome
Melorheostosis
Mulvihill-Smith syndrome
Neurocutaneous melanosis sequence
Neurofibromatosis type 1
Noonan syndrome
Panostotic fibrous dysplasia
Patterson syndrome
Peutz-Jeghers syndrome
Piebaldism
POEMS syndrome
Polyglandular autoimmune disease
Polyostotic fibrous dysplasia
Porphyria
Prader-Willi syndrome
Progeria
Proteus syndrome
Reflex sympathetic dystrophy syndrome
Romberg syndrome
Rothmund-Thomson syndrome
Saldino-Mainzer syndrome
Scurvy
Senter syndrome
Sézary syndrome
Silver-Russell syndrome
Speckled lentiginous nevus syndrome
Terminal osseous dysplasia-pigmentary defect
Trichorhinophalangeal dysplasia type 1
Trichorhinophalangeal dysplasia type 3
Tuberous sclerosis
Tuomaala syndrome
Turner syndrome
Tyrosinase-deficient oculocutaneous albinism
Vitamin A intoxication
Waardenburg syndrome
Watson syndrome
Weber-Christian syndrome
Wilson disease
Winchester syndrome
Wyburn-Mason syndrome
X-linked albinism and deafness

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