MeSH Browser

MeSH Supplementary: Contiguous Abcd1-Dxs1375e Deletion Syndrome
Unique ID: C564508
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564508
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; Gene Deletion; *Chromosome Disorders
Frequency: 1
Note: contiguous gene microdeletion syndrome involving ABCD1and BCAP31
Date of Entry: 2012/11/05
Revision Date: 2015/11/09

Contiguous Abcd1-Dxs1375e Deletion Syndrome MeSH Supplementary Concept Data 2025