MeSH Browser

MeSH Supplementary: Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema
Unique ID: C564538
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564538
Entry Term(s): OL-EDA-ID Syndrome; OLEDAID
Registry Numbers: 0
Previous Indexing: IMMUNOLOGIC DEFICIENCY SYNDROMES (2013-2019)
Heading Mapped to: *Ectodermal Dysplasia; *Lymphedema; *Osteopetrosis; *Genetic Diseases, X-Linked; *Primary Immunodeficiency Diseases
Frequency: 1
Note: mutation in NEMO gene
Date of Entry: 2012/11/05
Revision Date: 2019/06/17

Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema MeSH Supplementary Concept Data 2025