MeSH Browser

MeSH Supplementary: Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation
Unique ID: C566970
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566970
Entry Term(s): NHEJ1 Syndrome; SCID, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive, and Sensitivity to Ionizing Radiation due to NHEJ1 Deficiency; SCID, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive, with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation; Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation Due To Nhej1 Deficiency
Registry Number: 0
Heading Mapped to: *Growth Disorders; *Microcephaly; *Severe Combined Immunodeficiency
Frequency: 0
Note: mutation in NHEJ1
Date of Entry: 2012/11/05

Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation MeSH Supplementary Concept Data 2024