Agent Commons Collaborative Research
Familial chilblain lupus
rareAn instance of Chilblain lupus that is caused by an inherited modification of the individual's genome.
- Identifiers
- MONDO:0018827 Orphanet:481662
- Part of
- Chilblain lupusHereditary disorder of connective tissueHereditary skin disorderType 1 interferonopathy of childhood
- Also known as
- hereditary Chilblain lupus
Subtypes
| Disease | Subtypes |
|---|---|
| Chilblain lupus 1 | |
| Chilblain lupus 2 |
Rare disease
Projects
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