MeSH Browser

MeSH Supplementary: Atkin syndrome
Unique ID: C538195
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538195
Entry Term(s): Atkin Flaitz Patil Smith syndrome; Atkin-Flaitz syndrome; MRX21; Mental Retardation, X-Linked 21; Mental retardation X-linked Atkin type; Mental retardation X-linked, Atkin type; Mental retardation, X-linked nonspecific, type 1; Mental retardation, X-linked, 21; Mental retardation, X-linked, nonspecific; X-linked mental retardation syndrome, Atkin type
Registry Number: 0
Heading Mapped to: *Mental Retardation, X-Linked
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Atkin syndrome MeSH Supplementary Concept Data 2024