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Roifman-Chitayat Syndrome MeSH Supplementary Concept Data 2024


MeSH Supplementary
Roifman-Chitayat Syndrome
Unique ID
C567641
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567641
Entry Term(s)
Combined Immunodeficiency, Facial Dysmorphism, Optic Nerve Atrophy, Skeletal Anomalies, And Developmental Delay
Registry Number
0
Previous Indexing
IMMUNOLOGIC DEFICIENCY SYNDROMES (2013-2019)
Heading Mapped to
*Primary Immunodeficiency Diseases
*Bone Diseases, Developmental
Developmental Disabilities
*Optic Nerve Diseases
*Facies
Frequency
1
Date of Entry
2012/11/05
Revision Date
2019/06/17
Roifman-Chitayat Syndrome Preferred
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