Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Metabolic disease
/
Inborn errors of metabolism
/
Hereditary amyloidosis
/
Familial primary localized cutaneous amyloidosis
Amyloidosis, primary localized cutaneous, 3
rare
Identifiers
MONDO:0054765
OMIM:617920
Causal genes
GPNMB
Part of
Familial primary localized cutaneous amyloidosis
Also known as
PLCA3
Projects
Sign in to start a project
No projects yet.