primary localized cutaneous amyloidosis 1 Disease Ontology Browser

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Disease Ontology Browser

primary localized cutaneous amyloidosis 1 (DOID:0080930)
Alliance: disease page
Synonyms: familial primary localized cutaneous amyloidosis-1
Alt IDs: OMIM:105250
Definition: A primary cutaneous amyloidosis that has_material_basis_in heterozygous mutation in the gene encoding oncostatin M receptor-beta (OSMR) on chromosome 5p13.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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