MeSH Browser

MeSH Supplementary: Copper deficiency, familial benign
Unique ID: C535468
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535468
Entry Term(s): Familial benign copper deficiency; Familial benign hypocupremia
Registry Numbers: 0
Heading Mapped to: Copper / deficiency; *Hair Diseases; *Metabolism, Inborn Errors; *Dermatitis, Seborrheic; *Seizures
Frequency: 2
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Copper deficiency, familial benign MeSH Supplementary Concept Data 2025