non-syndromic X-linked intellectual disability

non-syndromic intellectual disability characterized by a X-linked inheritance pattern
rdfs:label
"non-syndromic X-linked intellectual disability"@en
skos:altLabel
"MENTAL RETARDATION, X-LINKED 23"@en
"MENTAL RETARDATION, X-LINKED 23; MRX23"@en
"MENTAL RETARDATION, X-LINKED 95"@en
"MRX"@en
"non-specific X-linked mental retardation"@en
"nonsyndromic X-linked mental retardation"@en
schema:description
"non-syndromic intellectual disability characterized by a X-linked inheritance pattern"@en
schema:dateModified "2026-10-24T00:34:00+00:00"^^xsd:dateTime
schema:version 2560166905
wikibase:identifiers 44
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p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0010230>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00480>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050776>
wdt:P14914 "D00777"
wdt:P1550 "777"
wdt:P2293 DMD
SYP
ARX
AGTR2
CLCN4
CSTF2
DDX3X
DLG3
ACSL4
FGF13
AFF2
GDI1
HCFC1
MECP2
PAK3
RPS6KA3
SYN1
TSPAN7
ZNF711
USP9X
OGT
CASK
ZMYM3
ARHGEF6
FRMPD4
MED12
MID2
IL1RAPL1
CNKSR2
IQSEC2
KIF4A
FTSJ1
SRPK3
RLIM
THOC2
STEEP1
UPF3B
ALG13
KLHL15
SLITRK2
SLC9A7
RAB39B
PTCHD1
ZDHHC15
BRWD3
NEXMIF
ZNF81
USP27X
wdt:P279 non-syndromic intellectual disability
X-linked intellectual disability
wdt:P2841 infantile onset
childhood onset
wdt:P2888 <http://identifiers.org/doid/DOID:0050776>
<http://purl.obolibrary.org/obo/DOID_0050776>
<http://www.orpha.net/ORDO/Orphanet_777>
wdt:P2892 "C0796229"
wdt:P31 type of disease
rare disease
wdt:P4317 "3542"
"5613"
wdt:P492 "300046"
"300047"
"300062"
"300114"
"300115"
"300143"
"300210"
"300271"
"300324"
"300355"
"300372"
"300387"
"300428"
"300433"
"300436"
"300454"
"300498"
"300505"
"300518"
"300558"
"300577"
"300659"
"300716"
"300802"
"300803"
"300844"
"300848"
"300849"
"300850"
"300851"
"300852"
"300912"
"300919"
"300923"
"309530"
"309549"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0010230"
wdt:P665 "H00480"
wdt:P699 "DOID:0050776"
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