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Renpenning syndrome 1 MeSH Supplementary Concept Data 2024


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
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 Preferred
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