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

Rare disease

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