Amyloidosis, primary localized cutaneous, 1

MONDO:0024522

Any primary cutaneous amyloidosis in which the cause of the disease is a mutation in the OSMR gene.

Also known as: OSMR primary cutaneous amyloidosis, PLCA1, amyloidosis 9, amyloidosis, primary cutaneous, 1, amyloidosis, primary localised cutaneous, type 1, amyloidosis, primary localized cutaneous, 1, amyloidosis, primary localized cutaneous, type 1, primary cutaneous amyloidosis caused by mutation in OSMR

3 clinical trials for this condition and its sub-types, 0 tagged with Amyloidosis, primary localized cutaneous, 1 itself.

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Part of

↑ Familial primary localized cutaneous amyloidosis (1)

Including sub-types (3) Tagged with Amyloidosis, primary localized cutaneous, 1 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.