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Familial chilblain lupus

MONDO:0018827

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

Also known as: hereditary Chilblain lupus, hereditary chilblain lupus

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

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Sub-types

Chilblain lupus 1 (0) Chilblain lupus 2 (0)

Broader categories

Cardiovascular disorder (1051) Disease (680) Autoimmune disease (305) Hereditary disease (176) Immune system disorder (148) Vascular disorder (135) Skin disorder (132) Rheumatic disorder (87) Connective tissue disorder (68) Cutaneous lupus erythematosus (36)

Trials to join now! 21 Not yet recruiting 6 Not yet finished but already full! 7 Completed 10 Terminated 1

Biopsy tolerance study ends early – what we know

Knowledge-focused Terminated

This study aimed to understand how well patients tolerate biopsies for autoimmune diseases and whether they feel properly informed. It planned to enroll 505 people but was terminated early. The results may help improve patient experience with these common procedures.

Sponsor: University Hospital, Brest • Aim: Knowledge-focused

Last updated Jun 28, 2026 00:00 UTC