DOID:0050776 - non-syndromic X-linked intellectual disability
A non-syndromic intellectual disability characterized by a X-linked inheritance pattern.
non-specific X-linked mental retardation
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
Disease Ontology ,
EMBL-EBI ,
OLSVis tree view ,
Ontobee
rps6ka3 ,
il1rapl1 ,
arx ,
slc9a7 ,
cnksr2 ,
rab39b ,
mecp2 ,
dmd.2 ,
agtr2 ,
tspan7 ,
syp ,
zdhhc15 ,
arhgef6 ,
clcn4 ,
znf711 ,
[+]
pak3 ,
ogt ,
dlg3 ,
upf3b ,
magt1 ,
klhl15 ,
usp9x ,
mid2 ,
brwd3 ,
ftsj1 ,
steep1 ,
dmd.3 ,
dmd.1 ,
gdi1 ,
kif4a ,
znf674 ,
acsl4 ,
iqsec2 ,
znf81 ,
nexmif ,
frmpd4 ,
hcfc1 ,
alg13
AGR ,
MGI ,
ZFIN ,
FlyBase ,
WormBase ,
RGD