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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

46 clinical trials for this condition and its sub-types, 2 tagged with Familial chilblain lupus itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary disorder of connective tissue (1314) ↑ Hereditary skin disorder (885) ↑ Type 1 interferonopathy of childhood (19) ↑ Chilblain lupus (3)

Sub-types of Familial chilblain lupus

Chilblain lupus 1 0 trials
Chilblain lupus 2 0 trials

Including sub-types (46) Tagged with Familial chilblain lupus (2)

Trials to join now! 1 Not yet finished but already full! 1

New drug hope for rare childhood immune disorders

Disease control Recruiting now

This early-stage trial tests a new medicine called IMSB301 in people with rare diseases where the immune system attacks the body. The study includes up to 6 participants aged 12 and older. The main goal is to check if the drug is safe and how it behaves in the body.

Phase 1 • Sponsor: ImmuneSensor Therapeutics Inc. • Aim: Disease control

Last updated Jun 27, 2026 08:13 UTC