Hypopigmentation of the skin
MONDO:0019290A 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
26 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Chediak-Higashi syndrome
(7)
Hermansky-Pudlak syndrome
(4)
Oculocutaneous albinism
(4)
Piebaldism
(4)
Griscelli syndrome
(1)
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)