primary localized cutaneous amyloidosis 1

Term ID

DOID:0080930

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. https://pubmed.ncbi.nlm.nih.gov/19663869/

References

• OMIM:105250

Ontology

Human Disease   ( DOID:0080930 )