MeSH Browser

MeSH Supplementary: Schindler Disease, Type I
Unique ID: C536631
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536631
Entry Term(s): Alpha-Galactosidase B Deficiency; Alpha-Galnac Deficiency, Schindler Type; Alpha-N-Acetylgalactosaminidase Deficiency; Alpha-N-Acetylgalactosaminidase Deficiency, Adult-Onset; Alpha-N-Acetylgalactosaminidase Deficiency, Type I; Alpha-N-Acetylgalactosaminidase Deficiency, Type III; Alpha-N-acetylgalactosaminidase deficiency adult onset; Alpha-N-acetylgalactosaminidase deficiency type 2; Alpha-N-acetylgalactosaminidase deficiency, type 1; Alpha-Naga Deficiency; Angiokeratoma Corporis Diffusum-Glycopeptiduria; Galb Deficiency; Kanzaki disease; Lysosomal Glycoaminoacid Storage Disease-Angiokeratoma Corporis Diffusum; NAGA Deficiency, Type II; NAGA Deficiency, Type III; NAGA deficiency type 2; Naga Deficiency; Naga Deficiency, Type I; Neuroaxonal dystrophy, Schindler type; Neuronal Axonal Dystrophy, Schindler Type; Schindler Disease; Schindler Disease, Type II; Schindler Disease, Type III; Schindler disease, type 1; Schindler disease, type 2; alpha-N-Acetylgalactosaminidase Deficiency, Type II
Registry Numbers: 0
Heading Mapped to: *Lysosomal Storage Diseases; *Neuroaxonal Dystrophies; alpha-N-Acetylgalactosaminidase / deficiency
Frequency: 4
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Schindler Disease, Type I MeSH Supplementary Concept Data 2025