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Lichen planus, familial

MONDO:0007902

An instance of lichen planus that is caused by an inherited modification of the individual's genome.

Also known as: hereditary lichen planus, lichen planus, familial

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

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Broader categories

Disease (680) Inflammatory disease (332) Hereditary disease (176) Skin disorder (132) Dermatitis (62) Lichen planus (16) Human disease (14) Hereditary skin disorder (6) Disease of genetic or genomic mechanism (2) Disease by body system or component (0)

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