Disease #00838 (MRXSR (mental retardation, X-linked syndromic, Raymond type (MRXSR)), OMIM:300799)

Official abbreviation MRXSR
Name mental retardation, X-linked syndromic, Raymond type (MRXSR)
OMIM ID 300799
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene ZDHHC9
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Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2019-02-26 21:28:48 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00147122 30631761-Pat46_S11 PubMed: Han 2018 - M no Korea - - - - - MRXSR developmental delay, no epilepsy, hypotonia ZDHHC9 ZDHHC9 1 1 Joonhong Park
00394439 patient PubMed: Ramos 2022, Journal: Ramos 2022 - M no Brazil - - - - - MRXSR see paper; ..., intellectual disability; early childhood severe growth failure, severe hypotonia, developmental delay; verbally aggressive, antisocial behavior - ZDHHC9 1 1 Juliana Mazzeu
00420838 206963 - - M no Italy - - - - - MRXSR Obesity, Macrocephaly, Delayed speech and language development, Intellectual disability, Macrotia, Dysarthria, Incisor macrodontia ZDHHC9 ZDHHC9 1 1 Andreas Laner
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