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Familial reactive perforating collagenosis
Disease definition
Familial reactive perforating collagenosis is a very rare genetic skin disease characterized by transepidermal elimination of collagen fibers presenting as recurrent spontaneously involuting keratotic papules or nodules.
ORPHA:79147
Classification level: Disorder- Synonym(s): -
- Prevalence: <1 / 1 000 000
- Inheritance: -
- Age of onset: Childhood
- ICD-10: L87.1
- OMIM: 216700
- UMLS: C1857624
- MeSH: -
- GARD: -
- MedDRA: -
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