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Roifman syndrome MeSH Supplementary Concept Data 2023


MeSH Supplementary
Roifman syndrome
Unique ID
C535866
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C535866
Entry Term(s)
Spondyloepiphseal dysplasia, retinal dystrophy, and antibody deficiency
Registry Number
0
Previous Indexing
IMMUNOLOGIC DEFICIENCY SYNDROMES (2013-2019)
Heading Mapped to
*Primary Immunodeficiency Diseases
*Cardiomyopathies
*Osteochondrodysplasias
*Retinal Diseases
*Mental Retardation, X-Linked
Frequency
11
Date of Entry
2010/08/25
Revision Date
2019/06/17
Roifman syndrome Preferred
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