primary localized cutaneous amyloidosis 1

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: osmr

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): primary cutaneous amyloidosis (is_a)