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Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema MeSH Supplementary Concept Data 2022


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 Number
0
Previous Indexing
IMMUNOLOGIC DEFICIENCY SYNDROMES (2013-2019)
Heading Mapped to
*Primary Immunodeficiency Diseases
*Ectodermal Dysplasia
*Lymphedema
*Osteopetrosis
*Genetic Diseases, X-Linked
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 Preferred
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