FB2025_05 , released December 11, 2025

CV Term Report

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General Information
Term	primary cutaneous amyloidosis	ID (Ontology)	DOID:0050639 (Human Disease)
Definition	An amyloidosis characterized by pruritus, skin scratching and by deposits of amyloid in the dermis.
Also Known As	"familial primary localized cutaneous amyloidosis" ; "PCA"
Comment
Links to External Ontologies
	DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Spanning Tree (Parents/Children)

disease of metabolism
 |__inherited metabolic disorder__
 |__amyloidosis___________________|
integumentary system disease      |
 |__skin disease__________________|
genetic disease                   |
 |__inherited metabolic disorder__|
                                  primary cutaneous amyloidosis  2 rec.
                                   |__Finnish type amyloidosis 2 rec.
                                   |__primary localized cutaneous amyloidosis 1
                                   |__primary localized cutaneous amyloidosis 2
                                   |__primary localized cutaneous amyloidosis 3

Spanning Tree View Settings
Parents/Children View Depth	Show hierarchy levels: for parents, for children
Relationships
Is a	skin disease inherited metabolic disorder amyloidosis
Part of
Synonyms & Secondary IDs
Synonyms
	"familial primary localized cutaneous amyloidosis" EXACT "PCA" EXACT OMO:0003012
Secondary IDs

External Crossreferences & Linkouts
	GARD:132 MIM:PS105250 ORDO:137807 ORDO:353220