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Summary Literature (0)
DOID:0050776 - non-syndromic X-linked intellectual disability


Disease Ontology Definition:A non-syndromic intellectual disability characterized by a X-linked inheritance pattern.

Synonyms: non-specific X-linked mental retardation

In OMIM:
OMIM:300143 - MENTAL RETARDATION, X-LINKED 21; MRX21
OMIM:300210 - MENTAL RETARDATION, X-LINKED 58; MRX58
OMIM:300387 - MENTAL RETARDATION, X-LINKED 63; MRX63
OMIM:300436 - MENTAL RETARDATION, X-LINKED 46; MRX46
OMIM:300498 - MENTAL RETARDATION, X-LINKED 45; MRX45
OMIM:300558 - MENTAL RETARDATION, X-LINKED 30; MRX30
OMIM:300577 - MENTAL RETARDATION, X-LINKED 91; MRX91
OMIM:300659 - MENTAL RETARDATION, X-LINKED 93; MRX93
OMIM:300716 - MENTAL RETARDATION, X-LINKED 95; MRX95
OMIM:300802 - MENTAL RETARDATION, X-LINKED 96; MRX96
OMIM:300803 - MENTAL RETARDATION, X-LINKED 97; MRX97
OMIM:300850 - MENTAL RETARDATION, X-LINKED 90; MRX90
OMIM:300912 - MENTAL RETARDATION, X-LINKED 98; MRX98
OMIM:300919 - MENTAL RETARDATION, X-LINKED 99; MRX99
OMIM:300923 - MENTAL RETARDATION, X-LINKED 100; MRX100
OMIM:309530 - MENTAL RETARDATION, X-LINKED 1; MRX1
OMIM:309549 - MENTAL RETARDATION, X-LINKED 9; MRX9

In Mondo Disease Ontology:
MONDO:0019181 - non-syndromic X-linked intellectual disability

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : rps6ka3, il1rapl1, arx, slc9a7, cnksr2, rab39b, mecp2, dmd.2, agtr2, tspan7, syp, zdhhc15, arhgef6, clcn4, znf711, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): X-linked disease (is_a), non-syndromic intellectual disability (is_a)