Term Name:	primary localized cutaneous amyloidosis 1
Synonyms:	familial primary localized cutaneous amyloidosis-1
Definition:	A primary cutaneous amyloidosis that has_material_basis_in heterozygous mutation in the gene encoding oncostatin M receptor-beta (OSMR) on chromosome 5p13.
Ontology:	Human Disease [DOID:0080930]   ( DOID:0080930 )