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- DiGeorge_syndrome abstract "22q11.2 deletion syndrome which has several presentations including DiGeorge syndrome (DGS), DiGeorge anomaly, velo-cardio-facial syndrome, Shprintzen syndrome, conotruncal anomaly face syndrome, Strong syndrome, congenital thymic aplasia, and thymic hypoplasia, is a syndrome caused by the deletion of a small piece of chromosome 22. The deletion occurs near the middle of the chromosome at a location designated 22q11.2—signifying its location on the long arm of one of the pair of chromosomes 22, on region 1, band 1, sub-band 2. The inheritance pattern is autosomal dominant and it has a prevalence estimated at 1:4000. The syndrome was described in 1968 by the pediatric endocrinologist Angelo DiGeorge. 22q11 deletion is also associated with truncus arteriosus (see TOF).".
- DiGeorge_syndrome diseasesdb "3631".
- DiGeorge_syndrome emedicineSubject "med".
- DiGeorge_syndrome emedicineTopic "567".
- DiGeorge_syndrome icd10 "D82.1".
- DiGeorge_syndrome icd9 "279.11, 758.32".
- DiGeorge_syndrome meshId "D004062".
- DiGeorge_syndrome omim "188400".
- DiGeorge_syndrome thumbnail Brain_computer_tomography_cuts_of_the_patient_with_22q11.2_syndrome,_demonstrating_basal_ganglia_and_periventricular_calcification.jpg?width=300.
- DiGeorge_syndrome wikiPageExternalLink ghr.nlm.nih.gov.
- DiGeorge_syndrome wikiPageExternalLink NBK1523.
- DiGeorge_syndrome wikiPageExternalLink NBK3823.
- DiGeorge_syndrome wikiPageExternalLink http://www.seattlechildrens.org/medical-conditions/chromosomal-genetic-conditions/velocardiofacial/#.
- DiGeorge_syndrome wikiPageExternalLink index.html.
- DiGeorge_syndrome wikiPageID "3724035".
- DiGeorge_syndrome wikiPageRevisionID "606802498".
- DiGeorge_syndrome caption "Brain computer tomography cuts of the patient, demonstrating basal ganglia and periventricular calcification. From a case report by Tonelli et al., 2007".
- DiGeorge_syndrome diseasesdb "3631".
- DiGeorge_syndrome emedicinesubj "med".
- DiGeorge_syndrome emedicinetopic "567".
- DiGeorge_syndrome hasPhotoCollection DiGeorge_syndrome.
- DiGeorge_syndrome icd "279.11".
- DiGeorge_syndrome icd "D82.1".
- DiGeorge_syndrome meshid "D004062".
- DiGeorge_syndrome name "22".
- DiGeorge_syndrome omim "188400".
- DiGeorge_syndrome subject Category:Autosomal_dominant_disorders.
- DiGeorge_syndrome subject Category:Autosomal_monosomies_and_deletions.
- DiGeorge_syndrome subject Category:IUIS-PID_table_3_immunodeficiencies.
- DiGeorge_syndrome subject Category:Noninfectious_immunodeficiency-related_cutaneous_conditions.
- DiGeorge_syndrome subject Category:Syndromes.
- DiGeorge_syndrome type Aberrance114503665.
- DiGeorge_syndrome type Abnormality114501726.
- DiGeorge_syndrome type Abstraction100002137.
- DiGeorge_syndrome type Attribute100024264.
- DiGeorge_syndrome type AutosomalDominantDisease114162025.
- DiGeorge_syndrome type AutosomalDominantDisorders.
- DiGeorge_syndrome type AutosomalMonosomiesAndDeletions.
- DiGeorge_syndrome type ChromosomalAberration114504103.
- DiGeorge_syndrome type Cognition100023271.
- DiGeorge_syndrome type Complex105870365.
- DiGeorge_syndrome type Concept105835747.
- DiGeorge_syndrome type Condition113920835.
- DiGeorge_syndrome type Content105809192.
- DiGeorge_syndrome type Disease114070360.
- DiGeorge_syndrome type Disorder114052403.
- DiGeorge_syndrome type GeneticDisease114151139.
- DiGeorge_syndrome type IUIS-PIDTable3Immunodeficiencies.
- DiGeorge_syndrome type Idea105833840.
- DiGeorge_syndrome type IllHealth114052046.
- DiGeorge_syndrome type Illness114061805.
- DiGeorge_syndrome type Immunodeficiency113974317.
- DiGeorge_syndrome type ImmunologicalDisorder113973990.
- DiGeorge_syndrome type Monosomy114504405.
- DiGeorge_syndrome type NoninfectiousImmunodeficiency-relatedCutaneousConditions.
- DiGeorge_syndrome type PathologicalState114051917.
- DiGeorge_syndrome type PhysicalCondition114034177.
- DiGeorge_syndrome type PsychologicalFeature100023100.
- DiGeorge_syndrome type State100024720.
- DiGeorge_syndrome type Syndrome105870790.
- DiGeorge_syndrome type Syndromes.
- DiGeorge_syndrome type Whole105869584.
- DiGeorge_syndrome type Disease.
- DiGeorge_syndrome type AilmentCondition.
- DiGeorge_syndrome type Situation.
- DiGeorge_syndrome comment "22q11.2 deletion syndrome which has several presentations including DiGeorge syndrome (DGS), DiGeorge anomaly, velo-cardio-facial syndrome, Shprintzen syndrome, conotruncal anomaly face syndrome, Strong syndrome, congenital thymic aplasia, and thymic hypoplasia, is a syndrome caused by the deletion of a small piece of chromosome 22.".
- DiGeorge_syndrome label "22q11.2欠失症候群".
- DiGeorge_syndrome label "DiGeorge syndrome".
- DiGeorge_syndrome label "Microdélétion 22q11".
- DiGeorge_syndrome label "Mikrodeletionsyndrom 22q11".
- DiGeorge_syndrome label "Sindrome da delezione 22q11".
- DiGeorge_syndrome label "Síndrome de DiGeorge".
- DiGeorge_syndrome label "Síndrome de DiGeorge".
- DiGeorge_syndrome label "Velo-cardio-faciaal syndroom".
- DiGeorge_syndrome label "Zespół delecji 22q11.2".
- DiGeorge_syndrome label "Синдром Ди Джорджи".
- DiGeorge_syndrome label "متلازمة دي جورج".
- DiGeorge_syndrome label "迪喬治症候群".
- DiGeorge_syndrome sameAs DiGeorgův_syndrom.
- DiGeorge_syndrome sameAs Mikrodeletionsyndrom_22q11.
- DiGeorge_syndrome sameAs Síndrome_de_DiGeorge.
- DiGeorge_syndrome sameAs Microdélétion_22q11.
- DiGeorge_syndrome sameAs Sindrom_delesi_22q11.
- DiGeorge_syndrome sameAs Sindrome_da_delezione_22q11.
- DiGeorge_syndrome sameAs 22q11.2欠失症候群.
- DiGeorge_syndrome sameAs 디조지_증후군.
- DiGeorge_syndrome sameAs Velo-cardio-faciaal_syndroom.
- DiGeorge_syndrome sameAs Zespół_delecji_22q11.2.
- DiGeorge_syndrome sameAs Síndrome_de_DiGeorge.
- DiGeorge_syndrome sameAs m.029k_.
- DiGeorge_syndrome sameAs Q525642.
- DiGeorge_syndrome sameAs Q525642.
- DiGeorge_syndrome sameAs 1169.
- DiGeorge_syndrome sameAs 263.
- DiGeorge_syndrome sameAs 321.
- DiGeorge_syndrome sameAs DiGeorge_syndrome.
- DiGeorge_syndrome wasDerivedFrom DiGeorge_syndrome?oldid=606802498.
- DiGeorge_syndrome depiction Brain_computer_tomography_cuts_of_the_patient_with_22q11.2_syndrome,_demonstrating_basal_ganglia_and_periventricular_calcification.jpg.
- DiGeorge_syndrome isPrimaryTopicOf DiGeorge_syndrome.
- DiGeorge_syndrome name "22q11.2 deletion syndrome".