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 2
Phenotype entries for this disease 2
Associated with 1 gene ZDHHC9
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00147122 30631761-Pat46_S11 PubMed: Han 2018 - M no Korea - - 0 - - MRXSR developmental delay, no epilepsy, hypotonia ZDHHC9 ZDHHC9 1 1 Joonhong Park
00394439 - - - M no Brazil - - - - - MRXSR intellectual disability, short stature - ZDHHC9 1 1 Juliana Mazzeu
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