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Chromosomal variation where a person is born with a 45X chromosome pattern rather than the typical 46XX

Property Value
dbo:description
  • homa malsano (eo)
  • مرض يصيب الإنسان (ar)
  • karyotypisch diagnostiziertes Syndrom (de)
  • Kondisi salah satu kromosom X yang sebagian atau seluruhnya hilang pada perempuan (in)
  • Aberrazio kromosomiko baten ondorioz sortzen den sindromea. Ia kasu guztietan emakumezkoan agertzen da eta ezaugarri nagusiak fenotipo femeninoak, altuera txikia, sexu-organo gutxi garatu eta antzuak, pubertaterik eza eta hainbat malformazio dira (eu)
  • Genetik bozukluk (tr)
  • chromosomale variantie van intersekse (nl)
  • 여성에게 X 염색체가 하나밖에 없어서 발생하는 증후군 (ko)
  • kromoszóma-rendellenesség (hu)
  • medfödd kromosonsjukdom (sv)
  • sindrome genetica umana (it)
  • trastorno cromosómico (gl)
  • vrozené onemocnění (cs)
  • স্ত্রীদেহের কোষে একটি এক্স ক্রোমোজোম অনুপস্থিত থাকার প্রকরণ (bn)
  • Rối loạn nhiễm sắc thể trong một phụ nữ có thể bị thiếu một phần hoặc hoàn toàn mất một nhiễm sắc thể X (vi)
  • 女性のみに起こる、2本のX染色体のうち1本の全体または一部が欠失していることによる先天性の性染色体疾患 (ja)
  • Γενετική ασθένεια (el)
  • хромосомная болезнь (ru)
  • naisilla ja tytöillä esiintyvä kromosomipoikkeavuus (fi)
  • نوعی ناهنجاری کروموزومی (fa)
  • генетична аномалія при якій частково або повністю відсутня Х-хромосома (uk)
  • ಮಾನವನ ಒಂದು ರೋಗ (kn)
  • chromosomal variation where a person is born with a 45X chromosome pattern rather than the typical 46XX (en)
dbo:diseasesDB
  • 13461
dbo:eMedicineSubject
  • ped (en)
dbo:eMedicineTopic
  • 2330 (en)
dbo:icd10
  • Q96.
dbo:icd9
  • 758.6
dbo:medicalDiagnosis
dbo:medlinePlus
  • 000379
dbo:meshId
  • D014424
dbo:orpha
  • 881
dbo:symptom
dbo:thumbnail
dbo:wikiPageExternalLink
dbo:wikiPageWikiLink
dbp:caption
  • Five Latina girls and women with Turner syndrome with wide neck and low-set ears (en)
dbp:causes
  • 1 (xsd:integer)
dbp:date
  • 2015-02-25 (xsd:date)
  • April 2016 (en)
dbp:diagnosis
dbp:diseasesdb
  • 13461 (xsd:integer)
dbp:displayAuthors
  • 6 (xsd:integer)
dbp:duration
  • Lifetime (en)
dbp:emedicinesubj
  • ped (en)
dbp:emedicinetopic
  • 2330 (xsd:integer)
dbp:field
dbp:frequency
  • 1 (xsd:integer)
dbp:icd
  • 758.600000 (xsd:double)
  • (en)
  • Q96. (en)
dbp:medlineplus
  • 379 (xsd:integer)
dbp:meshid
  • D014424 (en)
dbp:name
  • Turner syndrome (en)
dbp:nameListStyle
  • vanc (en)
dbp:namedAfter
dbp:onset
  • At birth (en)
dbp:onsetAlways
  • y (en)
dbp:orphanet
  • 881 (xsd:integer)
dbp:reason
  • use of association is non-standard (en)
dbp:risks
  • Nondisjunction in sperm (en)
dbp:symptoms
  • Neck webbing, short stature, heart defects, ptosis, cupped ears (en)
dbp:synonyms
  • Ullrich–Turner syndrome, X0 syndrome, 45,X, 45, X0 (en)
dbp:url
dbp:wikiPageUsesTemplate
dbp:wordnet_type
dct:subject
gold:hypernym
rdf:type
rdfs:label
  • Turner syndrome (en)
  • متلازمة تيرنر (ar)
  • Síndrome de Turner (ca)
  • Turnerův syndrom (cs)
  • Σύνδρομο Τέρνερ (el)
  • Turner-sindromo (eo)
  • Turner sindrome (eu)
  • Síndrome de Turner (es)
  • Turner-Syndrom (de)
  • Sindrom Turner (in)
  • Syndrome de Turner (fr)
  • ターナー症候群 (ja)
  • Sindrome di Turner (it)
  • 터너 증후군 (ko)
  • Zespół Turnera (pl)
  • Syndroom van Turner (nl)
  • Синдром Шерешевского — Тёрнера (ru)
  • Síndrome de Turner (pt)
  • Синдром Тернера (uk)
  • Turners syndrom (sv)
  • 特纳综合征 (zh)
owl:sameAs
prov:wasDerivedFrom
foaf:depiction
foaf:isPrimaryTopicOf
foaf:name
  • Turner syndrome (en)
is dbo:differentialDiagnosis of
is dbo:knownFor of
is dbo:wikiPageDisambiguates of
is dbo:wikiPageRedirects of
is dbo:wikiPageWikiLink of
is dbp:differential of
is foaf:primaryTopic of
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