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Familial acanthosis nigricans

MONDO:0043003

An instance of acanthosis nigricans (disease) that is caused by an inherited modification of the individual's genome.

Also known as: hereditary acanthosis nigricans (disease), acanthosis nigricans

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (717) Inflammatory disease (341) Hereditary disease (188) Skin disorder (135) Dermatitis (64) Human disease (15) Hereditary skin disorder (7) Acanthosis nigricans (4) Disease of genetic or genomic mechanism (2) Disease by body system or component (0)

Not yet recruiting 1

Can immune fingerprints unlock new treatments for skin disease?

Knowledge-focused Not yet recruiting

This observational study aims to map the immune and molecular profiles of people with inflammatory skin conditions, including genetic forms like epidermolysis bullosa. By comparing these profiles to those of healthy individuals, researchers hope to identify unique signatures that…

Sponsor: Guy's and St Thomas' NHS Foundation Trust • Aim: Knowledge-focused

Last updated Aug 20, 2026 00:00 UTC