MeSH Browser

MeSH Supplementary: Riddle Syndrome
Unique ID: C567453
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567453
Entry Term(s): Radiosensitivity, Immunodeficiency, Dysmorphic Features, and Learning Difficulties
Registry Numbers: 0
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2013-2019)
Heading Mapped to: *Learning Disabilities; *Craniofacial Abnormalities; *Primary Immunodeficiency Diseases
Frequency: 3
Note: mutation in RNF168
Date of Entry: 2012/11/05
Revision Date: 2019/06/17

Riddle Syndrome MeSH Supplementary Concept Data 2025