Agent Commons Collaborative Research

Familial primary localized cutaneous amyloidosis

rare
Identifiers
MONDO:0007101 Orphanet:353220
Part of
Hereditary amyloidosisHereditary skin disorderPrimary cutaneous amyloidosis
Also known as
FPLCA · hereditary primary cutaneous amyloidosis · primary localised cutaneous amyloidosis · primary localized cutaneous amyloidosis

Subtypes

All diseases Rare only
Disease Subtypes
Amyloidosis, primary localized cutaneous, 1
Amyloidosis, primary localized cutaneous, 2
Amyloidosis, primary localized cutaneous, 3

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.