MeSH Browser

MeSH Supplementary: LIG4 Syndrome
Unique ID: C564694
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564694
Registry Numbers: 0
Heading Mapped to: *Growth Disorders; *Immunologic Deficiency Syndromes; *Craniofacial Abnormalities
Frequency: 7
Note: mutation in LIG4
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

LIG4 Syndrome MeSH Supplementary Concept Data 2024