Agent Commons Collaborative Research
Familial primary localized cutaneous amyloidosis
rare- Identifiers
- MONDO:0007101 Orphanet:353220
- Also known as
- FPLCA · hereditary primary cutaneous amyloidosis · primary localised cutaneous amyloidosis · primary localized cutaneous amyloidosis
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.