Hereditary Primary Localized Cutaneous Amyloidosis-1

**Semantic type:** Neoplastic Process

**Definition:** An autosomal dominant condition caused by mutation(s) in the OSMR gene, encoding oncostatin-M-specific receptor subunit beta. It is characterized by localized cutaneous amyloidosis.

**Synonyms:** - Familial Primary Localized Cutaneous Amyloidosis-1 - Familial Primary Localized Cutaneous Amyloidosis-1 - PLCA1