Roifman syndrome [Supplementary Concept]

Date introduced: August 25, 2010

MeSH Unique ID: C535866

Heading Mapped to:

• Primary Immunodeficiency Diseases
• Cardiomyopathies
• Osteochondrodysplasias
• Retinal Diseases
• Mental Retardation, X-Linked

Entry Terms:

• Spondyloepiphseal dysplasia, retinal dystrophy, and antibody deficiency

Previous Indexing:

• IMMUNOLOGIC DEFICIENCY SYNDROMES (2013-2019)