MeSH Browser

MeSH Supplementary: Pigmentary Disorder, Reticulate, with Systemic Manifestations
Unique ID: C564461
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564461
Entry Term(s): Amyloidosis, Familial Cutaneous
Registry Numbers: 0
Heading Mapped to: *Pigmentation Disorders; *Skin Diseases, Genetic; *Amyloidosis, Familial; *Genetic Diseases, X-Linked
Frequency: 5
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Pigmentary Disorder, Reticulate, with Systemic Manifestations MeSH Supplementary Concept Data 2025