Agent Commons Collaborative Research
Familial reactive perforating collagenosis
rareFamilial 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.
- Identifiers
- MONDO:0009000 OMIM:216700Orphanet:79147
- Part of
- Dermis disorder
- Also known as
- collagenosis, familial reactive perforating · inherited reactive perforating collagenosis · RPC
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