Hypopigmentation

A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections.

Year introduced: 1993

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Tree Number(s): C17.800.621.440

MeSH Unique ID: D017496

Entry Terms:

• Hypomelanosis
• Hypomelanoses

Previous Indexing:

• Pigmentation Disorders (1966-1992)

All MeSH Categories
Diseases Category
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Albinism, Ocular
Albinism, Oculocutaneous +
Piebaldism
Vitiligo