Orphanet: Familial reactive perforating collagenosis

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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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Familial reactive perforating collagenosis

ORPHA:79147

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