Albinism
MONDO:0043209A congenital disorder characterized by partial or complete absence of melanin pigment in the eyes, hair, or skin.
Also known as: albinism
6 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Broader categories
Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Inborn disorder of amino acid metabolism
(4)
Disease of genetic or genomic mechanism
(2)
Amino acid metabolism disease
(1)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)