Hypopigmentation of the skin

MONDO:0019290

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.

Also known as: hypopigmentation of the skin, hypopigmentation of the skin (disease), hypomelanoses, hypomelanosis

21 clinical trials for this condition and its sub-types.

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Sub-types

Chediak-Higashi syndrome (9) Hermansky-Pudlak syndrome (4) Oculocutaneous albinism (4) Piebaldism (4) Griscelli syndrome (2) Griscelli syndrome type 2 (1) Hermansky-Pudlak syndrome 1 (1) Hermansky-Pudlak syndrome 4 (1) Oculocutaneous albinism type 1A (1) Tietz syndrome (1) Albinism-hearing loss syndrome (0) Autosomal dominant oculocutaneous albinism (0) Deaf blind hypopigmentation syndrome, Yemenite type (0) Deafness, congenital, with total albinism (0) Griscelli syndrome type 1 (0) Griscelli syndrome type 3 (0) Hermansky-Pudlak syndrome 10 (0) Hermansky-Pudlak syndrome 11 (0) Hermansky-Pudlak syndrome 2 (0) Hermansky-Pudlak syndrome 3 (0)

Broader categories

Disease (680) Skin disorder (132) Human disease (14) Skin pigmentation disorder (11) Disease by body system or component (0) Integumentary system disorder (0)

Trials to join now! 12 Not yet recruiting 2 Not yet finished but already full! 5 Completed 2

Hypopigmentation of the skin

Sub-types

Broader categories

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