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- WAGR_syndrome abstract "WAGR syndrome is a rare genetic syndrome in which affected children are predisposed to develop Wilms tumour (a tumour of the kidneys), Aniridia (absence of the coloured part of the eye, the iris), Genitourinary anomalies, and Retardation. The G is sometimes instead given as "gonadoblastoma," since the genitourinary anomalies are tumours of the gonads (testes or ovaries).A subset of WAGR syndrome patients shows severe childhood obesity; the acronym WAGRO (O for obesity) has been used to describe this category.The condition results from a deletion on chromosome 11 resulting in the loss of several genes. As such, it is one of the best studied examples of a condition caused by loss of neighbouring (contiguous) genes.".
- WAGR_syndrome diseasesdb "14025".
- WAGR_syndrome emedicineSubject "ped".
- WAGR_syndrome emedicineTopic "2423".
- WAGR_syndrome meshId "D017624".
- WAGR_syndrome omim "194072".
- WAGR_syndrome wikiPageExternalLink www.wagr.org.
- WAGR_syndrome wikiPageID "3186837".
- WAGR_syndrome wikiPageRevisionID "600096935".
- WAGR_syndrome diseasesdb "14025".
- WAGR_syndrome emedicinesubj "ped".
- WAGR_syndrome emedicinetopic "2423".
- WAGR_syndrome hasPhotoCollection WAGR_syndrome.
- WAGR_syndrome meshid "D017624".
- WAGR_syndrome name "WAGR syndrome".
- WAGR_syndrome omim "194072".
- WAGR_syndrome wordnet_type synset-disease-noun-1.
- WAGR_syndrome subject Category:Autosomal_monosomies_and_deletions.
- WAGR_syndrome subject Category:Syndromes.
- WAGR_syndrome type Aberrance114503665.
- WAGR_syndrome type Abnormality114501726.
- WAGR_syndrome type Abstraction100002137.
- WAGR_syndrome type Attribute100024264.
- WAGR_syndrome type AutosomalMonosomiesAndDeletions.
- WAGR_syndrome type ChromosomalAberration114504103.
- WAGR_syndrome type Cognition100023271.
- WAGR_syndrome type Complex105870365.
- WAGR_syndrome type Concept105835747.
- WAGR_syndrome type Condition113920835.
- WAGR_syndrome type Content105809192.
- WAGR_syndrome type Disease114070360.
- WAGR_syndrome type Idea105833840.
- WAGR_syndrome type IllHealth114052046.
- WAGR_syndrome type Illness114061805.
- WAGR_syndrome type Monosomy114504405.
- WAGR_syndrome type PathologicalState114051917.
- WAGR_syndrome type PhysicalCondition114034177.
- WAGR_syndrome type PsychologicalFeature100023100.
- WAGR_syndrome type State100024720.
- WAGR_syndrome type Syndrome105870790.
- WAGR_syndrome type Syndromes.
- WAGR_syndrome type Whole105869584.
- WAGR_syndrome type Disease.
- WAGR_syndrome type AilmentCondition.
- WAGR_syndrome type Situation.
- WAGR_syndrome comment "WAGR syndrome is a rare genetic syndrome in which affected children are predisposed to develop Wilms tumour (a tumour of the kidneys), Aniridia (absence of the coloured part of the eye, the iris), Genitourinary anomalies, and Retardation.".
- WAGR_syndrome label "Sindrome WAGR".
- WAGR_syndrome label "Síndrome WAGR".
- WAGR_syndrome label "WAGR syndrome".
- WAGR_syndrome label "WAGR-Syndrom".
- WAGR_syndrome label "Zespół WAGR".
- WAGR_syndrome sameAs WAGR-Syndrom.
- WAGR_syndrome sameAs Síndrome_WAGR.
- WAGR_syndrome sameAs Sindrome_WAGR.
- WAGR_syndrome sameAs Zespół_WAGR.
- WAGR_syndrome sameAs m.08xx_2.
- WAGR_syndrome sameAs Q1892153.
- WAGR_syndrome sameAs Q1892153.
- WAGR_syndrome sameAs 1183.
- WAGR_syndrome sameAs WAGR_syndrome.
- WAGR_syndrome wasDerivedFrom WAGR_syndrome?oldid=600096935.
- WAGR_syndrome isPrimaryTopicOf WAGR_syndrome.
- WAGR_syndrome name "WAGR syndrome".