SHMARQL

triploid syndrome

<http://www.wikidata.org/entity/Q56137331>

extremely rare chromosomal disorder occuring during human embryogenesis, causing severe abnormalities in fetal development and usually lethal in the prenatal stage
rdfs:label
"triploid syndrome"@en
skos:altLabel
"chromosome triploidy syndrome"@en
"triploidy"@en
"triploidy syndrome"@en
schema:description
"extremely rare chromosomal disorder occuring during human embryogenesis, causing severe abnormalities in fetal development and usually lethal in the prenatal stage"@en
schema:dateModified "2026-10-24T00:09:25+00:00"^^xsd:dateTime
schema:version 2560162983
wikibase:identifiers 13
15
wikibase:sitelinks 6
wikibase:statements 49
p:P14914 wd:statement/Q56137331-55ACB0DA-B5AD-4D16-9AA0-76EF8AAC8052
p:P1550 wd:statement/Q56137331-7c49c4a0-45ff-a636-54d2-de95ed027bf3
p:P1692 wd:statement/Q56137331-4c23535e-4be9-d14d-4755-bbcf489ed476
p:P1748 wd:statement/Q56137331-b31e4a8a-4cbb-9e43-c870-63f0d8190e53
p:P1995 wd:statement/Q56137331-1AA46939-D749-47CD-A242-1D6CF7AD8FF8
p:P279 wd:statement/Q56137331-34471838-4475-bfba-c27b-d0041130062f
wd:statement/Q56137331-F908150F-C485-4C97-BC15-85E8AA84893E
wd:statement/Q56137331-a90d4de5-448c-46e9-3c92-df37303f7ab3
wd:statement/Q56137331-d6d286e4-4038-7102-8801-895c0e7aa408
p:P2841 wd:statement/Q56137331-A7A3D005-112D-4F3D-A517-A7946981AC22
wd:statement/Q56137331-BCC6425B-BC95-4ACB-9B77-BDAE8C4E4197
p:P2888 wd:statement/Q56137331-26A393A3-25DA-405B-955F-9E79FB51B0CF
p:P2892 wd:statement/Q56137331-52b16637-43b0-3850-df12-521ba0f3a413
p:P31 wd:statement/Q56137331-E9A2B9E1-C022-49FD-BFD7-B16DC5B0598D
p:P4229 wd:statement/Q56137331-44dd4872-48f5-c622-3c9b-036c18c56620
p:P4317 wd:statement/Q56137331-6208a9fb-41da-75e5-ae02-cc08b7e1b953
p:P486 wd:statement/Q56137331-9653c0e1-4279-954c-63b8-9c3454e7e694
p:P5270 wd:statement/Q56137331-56293C7D-74D0-4BEE-B833-B8BF114A71A2
p:P557 wd:statement/Q56137331-915EFE54-DF60-4023-85EB-4CE7E95C3DCC
p:P6366 wd:statement/Q56137331-B97DA148-41F9-400A-AB38-4CDF0B9E3ABC
p:P6532 wd:statement/Q56137331-033A5D0C-F77B-4E16-87F4-8736EBB91284
wd:statement/Q56137331-050A2512-44AC-46F7-8F60-740EDF2CC5F6
wd:statement/Q56137331-11D4D91C-97C8-4A51-B41C-9FFF3931D845
wd:statement/Q56137331-14758DC4-FB77-4BFB-A6A3-57D07FBBE059
wd:statement/Q56137331-181C06AF-6190-4C1A-81A2-841DE82CC181
wd:statement/Q56137331-1CBF46C3-0AA0-48C1-BB25-9B51BCFF90BF
wd:statement/Q56137331-227125DC-8D80-42CE-9C6E-EB7D4FEAB9FD
wd:statement/Q56137331-2453FE1C-BB2C-42BB-931B-DC3061C95ECA
wd:statement/Q56137331-439B43AF-8A12-4526-BB1A-54488551920D
wd:statement/Q56137331-5920C1D7-01B6-4285-8291-F302D94D8833
wd:statement/Q56137331-79C8D89E-64F9-4FCB-9BC8-6EAE0CFEAB03
wd:statement/Q56137331-A0AC670B-C91C-4C1B-B7D6-898BBCA4873F
wd:statement/Q56137331-B7B9E595-5F32-4CBF-9F6E-88772F3DE6E1
wd:statement/Q56137331-BAF9B12E-D4A2-42EE-A4BE-D1EEEB20C407
wd:statement/Q56137331-C9EB31D5-417A-4655-9EF8-5E2F9305228A
wd:statement/Q56137331-D429D0E5-CC67-425C-BF86-DB64262E5F37
wd:statement/Q56137331-DC6F1463-C7FF-4528-ACF9-B807D890F9A9
wd:statement/Q56137331-E765BA03-ED05-4DD5-96C1-AE34368C74CC
wd:statement/Q56137331-EB34008B-5FC2-4186-A6C7-F761D11F833C
wd:statement/Q56137331-EF57784D-7F34-4232-9E6E-79EA2BF7E718
wd:statement/Q56137331-F49D1C16-59E2-41D8-BBCB-514FA8169E9F
wd:statement/Q56137331-F7BC3F3D-7B40-4726-881B-94DABCDAB0B7
wd:statement/Q56137331-FBD44503-555E-4143-81CC-31769430F7FA
p:P672 wd:statement/Q56137331-1956a470-4975-a57b-a340-3ea084f5c1f8
wd:statement/Q56137331-21bb4582-48f8-1653-163d-c148628ce15b
wd:statement/Q56137331-7c2a6ac8-4bdb-5c84-7e24-67b21a9359f0
p:P7329 wd:statement/Q56137331-C457F367-170F-4EE0-875F-B44E1BF3C524
p:P7807 wd:statement/Q56137331-4E3F05D7-0796-4AE7-9B32-035DE460C2DB
p:P828 wd:statement/Q56137331-70e61749-4724-33c2-69d1-238624fd571f
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D057885>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0018067>
p:direct-normalized/P6366 <https://makg.org/entity/2778419287>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C23.550.210.702.500>
<http://id.nlm.nih.gov/mesh/G05.365.590.175.677.500>
<http://id.nlm.nih.gov/mesh/G05.700.740.500>
wdt:P14914 "D03376"
wdt:P1550 "3376"
wdt:P1692 "758.89"
wdt:P1748 "C85204"
wdt:P1995 medical genetics
wdt:P279 syndromic obesity
chromosomal anomaly with cataract
wdt:P2841 congenital onset
neonatal onset
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_3376>
wdt:P2892 "C0333693"
wdt:P31 type of disease
wdt:P4229 "Q92.7"
wdt:P4317 "5295"
wdt:P486 "D057885"
wdt:P5270 "MONDO_0018067"
wdt:P557 "32658"
wdt:P6366 "2778419287"
wdt:P6532 macrostomia
micrognathism
hypospadias
meningocele
cataract
hepatomegaly
Abnormality of chromosome segregation
Non-midline cleft of the upper lip
holoprosencephaly
micropenis
hypertelorism
heart septal defect
hydrocephalus
cleft palate
Intestinal malrotation
macroglossia
disorder of sex development
coloboma of iris
macrocephaly
microstomia
pancreas disease
cryptorchidism
polyhydramnios
wdt:P672 "C23.550.210.702.500"
"G05.365.590.175.677.500"
"G05.700.740.500"
wdt:P7329 "LD42.0"
wdt:P7807 "1900317965"
wdt:P828 triploidy
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data from SPARQL profile: Wikidata