SHMARQL

FG syndrome

<http://www.wikidata.org/entity/Q530142>

disease
rdfs:label
"FG syndrome"@en
skos:altLabel
"FG syndrome type 1"@en
"Fg Syndrome"@en
"Fg Syndrome 1"@en
"Keller syndrome"@en
"Mental Retardation, Large Head, Imperforate Anus, Congenital Hypotonia, and Partial Agenesis of Corpus Callosum"@en
"OKS"@en
"OPITZ-KAVEGGIA SYNDROME; OKS"@en
"Opitz-Kaveggia syndrome"@en
"Opitz–Kaveggia syndrome"@en
schema:description
"disease"@en
schema:dateModified "2026-10-24T00:45:06+00:00"^^xsd:dateTime
schema:version 2560168543
wikibase:identifiers 22
24
wikibase:sitelinks 9
wikibase:statements 38
p:P11143 wd:statement/Q530142-FF17412C-08E0-4DE0-A8A2-36523D1AE353
p:P11430 wd:statement/Q530142-712b8ae0-4d83-128f-b449-44d92cf3480d
p:P11956 wd:statement/Q530142-6993375D-001A-4B37-BE15-08F0A1DB904C
p:P138 wd:statement/q530142-5B32112B-3803-476D-A303-5D8933DA2B98
p:P14914 wd:statement/Q530142-CFCF0545-A3A8-4FFF-B948-B797111A69FE
p:P1550 wd:statement/Q530142-93736006-4348-9451-20cf-b1c9912a72b0
p:P1748 wd:statement/Q530142-cadf2b32-47fe-63af-6520-5d14bc37f516
p:P2293 wd:statement/Q530142-61E52ADF-58F6-4D24-AC09-FA2C5E088CBA
wd:statement/Q530142-C3D6E30F-C079-42C0-A5AA-1AF2B65B4A12
wd:statement/Q530142-D434DBFF-3502-4389-A81F-B3B0F64CC5DF
p:P279 wd:statement/Q530142-9175F168-E9C5-498B-B23B-9628F994B431
wd:statement/Q530142-C6EBFB75-A389-4ADE-A74E-A5A3605F9344
p:P2841 wd:statement/Q530142-47A87C32-00B5-4A68-A573-250F4A087AA5
wd:statement/Q530142-8A55FFE9-A621-4C32-B000-46598342074D
p:P2888 wd:statement/Q530142-A4D897C0-F33D-4FFF-9B3A-C968AE83AD38
wd:statement/Q530142-EBB6AC78-29A3-4414-83B3-F21B19D3F121
p:P2892 wd:statement/Q530142-418D733B-DEAA-4A73-8D3F-FB91CB375182
p:P31 wd:statement/Q530142-6D76F953-8F55-4831-B263-9E53B8AA9B27
wd:statement/Q530142-F41D9DF6-0B33-4F68-955C-9F9A4FB3B289
p:P3417 wd:statement/Q530142-1A8E518A-37DA-4016-BBA4-0CE9ECC0C67E
p:P4233 wd:statement/Q530142-866014b0-45e6-98a2-1bcd-75f159522838
p:P4317 wd:statement/Q530142-0BFEF3BD-B1C2-446B-A783-1A7648B96C5E
p:P486 wd:statement/Q530142-7C729500-9932-433D-9C51-457720E8AC5E
p:P492 wd:statement/Q530142-2E61E2B4-C680-43AF-831C-EC220D801EC9
wd:statement/Q530142-70426361-D3F8-4DD6-B8C9-3C38AB679C15
wd:statement/Q530142-8AE82AC4-1E5C-4964-9AB9-A84F7C037479
wd:statement/Q530142-E7DF1D28-B022-4F93-8F88-9DAC9725BEA2
wd:statement/Q530142-F5AE98E2-B46C-46A6-BAEC-224CD76D1A85
p:P5008 wd:statement/Q530142-33E77280-C987-47F1-8C0E-9704BDF4371B
p:P5270 wd:statement/Q530142-9F9C7D2B-E386-4D1F-8783-626BB8E3876B
p:P557 wd:statement/q530142-DF33FAF4-46B8-4942-8E6A-5588CDF28D33
p:P6366 wd:statement/Q530142-5EA94983-1E7F-4388-ABD1-AA3DAA790B32
p:P646 wd:statement/Q530142-3C0EB542-3A47-4397-8CC0-84E50F767F89
p:P6532 wd:statement/Q530142-E61D21F3-1A23-4D8C-9586-942747731847
p:P665 wd:statement/Q530142-3DD78392-4C96-445B-8283-00CE47362551
p:P668 wd:statement/q530142-37FAD3E9-D352-4CC0-84B3-AAFC898A59EE
p:P699 wd:statement/Q530142-58BAB538-6AF3-451D-B72F-A2D062CD489C
p:P7464 wd:statement/Q530142-8247CF7F-BE48-4C08-A1E4-734FE4325EFB
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/C537923>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0010590>
p:direct-normalized/P6366 <https://makg.org/entity/2777901717>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00894>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:14711>
wdt:P11143 "FG syndrome"
wdt:P11430 "DI-02095"
wdt:P11956 "0009297"
wdt:P138 John Marius Opitz
wdt:P14914 "D93932"
wdt:P1550 "93932"
wdt:P1748 "C171270"
wdt:P2293 FLNA
CASK
MED12
wdt:P279 syndrome
X-linked recessive disease
wdt:P2841 congenital onset
neonatal onset
wdt:P2888 <http://identifiers.org/doid/DOID:14711>
<http://purl.obolibrary.org/obo/DOID_14711>
wdt:P2892 "C0220769"
wdt:P31 type of disease
rare disease
wdt:P3417 "FG-Syndrome"
wdt:P4233 "fgs"
wdt:P4317 "2317"
wdt:P486 "C537923"
wdt:P492 "300321"
"300406"
"300422"
"300581"
"305450"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0010590"
wdt:P557 "32162"
wdt:P6366 "2777901717"
wdt:P646 "/m/051whx6"
wdt:P6532 seizure
wdt:P665 "H00894"
wdt:P668 "NBK1676"
wdt:P699 "DOID:14711"
wdt:P7464 "fg-syndrome"
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