Category:Disturbances of human pigmentation
Wikimedia Commons has media related to Disorders of pigmentation.
 | This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes L80-L81 within Chapter XII: Diseases of the skin and subcutaneous tissue should be included in this category. |
Disturbances of human pigmentation, either loss or reduction, may be related to loss of melanocytes or the inability of melanocytes to produce melanin or transport melanosomes correctly.
Subcategories
This category has only the following subcategory.
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Pages in category "Disturbances of human pigmentation"
The following 119 pages are in this category, out of 119 total. This list may not reflect recent changes.
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- ABCD syndrome
- Acromelanism
- Albinism – black lock – cell migration disorder of the neurocytes of the gut – deafness syndrome
- Albinism in humans
- Albinism–black lock–cell migration disorder of the neurocytes of the gut–deafness syndrome
- Albinism–deafness syndrome
- Alezzandrini syndrome
- Argyria
- Arsenic poisoning
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G
H
L
M
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- Pallister–Killian syndrome
- Partial albinism with immunodeficiency
- Partington amyloidosis
- Partington cutaneous amyloidosis
- Partington syndrome type II
- Pegum syndrome
- Periorbital hyperpigmentation
- Peutz–Jeghers syndrome
- Photoleukomelanodermatitis of Kobori
- Phylloid hypomelanosis
- Piebaldism
- Pigmentatio reticularis faciei et colli
- Pityriasis alba
- Poikiloderma
- Poikiloderma of Civatte
- Poikiloderma vasculare atrophicans
- Postinflammatory hypermelanosis
- Postinflammatory hyperpigmentation
- Postinflammatory hypopigmentation
- Progressive macular hypomelanosis