MeSH Browser

MeSH Supplementary: Renpenning syndrome 1
Unique ID: C537761
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537761
Entry Term(s): Golabi-Ito-Hall Syndrome; Hamel Cerebropalatocardiac Syndrome; MRXS3; MRXS8; Mental Retardation, X-Linked 55; Mental Retardation, X-Linked, Renpenning Type; Mental Retardation, X-Linked, Syndromic 3; Mental Retardation, X-Linked, With Spastic Diplegia; Mental retardation, X-linked Renpenning type; Mental retardation, X-linked, syndromic 8; Mrx55; Porteous Syndrome; RENS1; Renpenning Syndrome; Sutherland-Haan X-linked mental retardation syndrome; Sutherland-Haan syndrome; X-Linked Intellectual Deficit Due To Pqbp1 Mutations; X-Linked Intellectual Deficit, Renpenning Type; X-linked mental retardation syndromic 3; X-linked mental retardation with spastic diplegia
Registry Number: 0
Heading Mapped to: *Cerebral Palsy; *Mental Retardation, X-Linked
Frequency: 15
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Renpenning syndrome 1 MeSH Supplementary Concept Data 2023