Disease #00822 (MRX1 (mental retardation, X-linked, type 1), OMIM:309530)

Official abbreviation MRX1
Name mental retardation, X-linked, type 1
OMIM ID 309530
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease 3
Phenotype entries for this disease 1
Associated with 1 gene IQSEC2
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Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00391755 154312 - - M no Germany - - - - - MRX1 Myoclonus, Absent speech, Atypical absence seizure, Multifocal epileptiform discharges, Severe global developmental delay IQSEC2 IQSEC2 1 1 Andreas Laner
00391856 223P - - F no Spain - - - - - ID, MRX1 - - IQSEC2 1 1 Alejandro Brea-Fernández
00391863 031P - - M no Spain - - - - - ID, MRX1, MRX94 - - GRIA3 1 1 Alejandro Brea-Fernández
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