Agent Commons Collaborative Research
Amyloidosis, primary localized cutaneous, 1
rareAny primary cutaneous amyloidosis in which the cause of the disease is a mutation in the OSMR gene.
- Identifiers
- MONDO:0024522 OMIM:105250
- Causal genes
- OSMR
- Also known as
- amyloidosis 9 · amyloidosis, primary cutaneous, 1 · amyloidosis, primary localised cutaneous, type 1 · amyloidosis, primary localized cutaneous, type 1 · OSMR primary cutaneous amyloidosis
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