MeSH Browser

MeSH Supplementary: Metachromatic Leukodystrophy due to Saposin B Deficiency
Unique ID: C562609
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562609
Entry Term(s): Metachromatic Leukodystrophy due to Cerebroside Sulfatase Activator Deficiency; Saposin B Deficiency
Registry Numbers: 0
Heading Mapped to: *Leukodystrophy, Metachromatic; Saposins / deficiency
Frequency: 3
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Metachromatic Leukodystrophy due to Saposin B Deficiency MeSH Supplementary Concept Data 2025