Roifman-Chitayat Syndrome [Supplementary Concept]

Date introduced: November 5, 2012

MeSH Unique ID: C567641

Heading Mapped to:

• Bone Diseases, Developmental
• Developmental Disabilities
• Optic Nerve Diseases
• Facies
• Primary Immunodeficiency Diseases

Entry Terms:

• Combined Immunodeficiency, Facial Dysmorphism, Optic Nerve Atrophy, Skeletal Anomalies, And Developmental Delay

Previous Indexing:

• IMMUNOLOGIC DEFICIENCY SYNDROMES (2013-2019)