MeSH Browser

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 MeSH Supplementary Concept Data 2024