Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0080930 - primary localized cutaneous amyloidosis 1

Disease Ontology Definition:A primary cutaneous amyloidosis that has_material_basis_in heterozygous mutation in the gene encoding oncostatin M receptor-beta (OSMR) on chromosome 5p13.

Synonyms: familial primary localized cutaneous amyloidosis-1

Xenbase Genes : osmr


MIM:
MIM:105250 - AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; PLCA1

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): primary cutaneous amyloidosis (is_a)