About: Chromosomal deletion syndrome

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Chromosomal deletion syndromes result from deletion of parts of chromosomes. Depending on the location, size, and whom the deletion is inherited from, there are a few known different variations of chromosome deletions. Chromosomal deletion syndromes typically involve larger deletions that are visible using karyotyping techniques. Smaller deletions result in Microdeletion syndrome, which are detected using fluorescence in situ hybridization (FISH)

Attributes	Values
rdf:type	Thing Disease yago:WikicatAutosomalMonosomiesAndDeletions yago:Aberrance114503665 yago:Abnormality114501726 yago:Abstraction100002137 yago:Attribute100024264 yago:ChromosomalAberration114504103 yago:Condition113920835 yago:Monosomy114504405 yago:PhysicalCondition114034177 disease yago:State100024720
rdfs:label	Chromosomal deletion syndrome (en)
rdfs:comment	Chromosomal deletion syndromes result from deletion of parts of chromosomes. Depending on the location, size, and whom the deletion is inherited from, there are a few known different variations of chromosome deletions. Chromosomal deletion syndromes typically involve larger deletions that are visible using karyotyping techniques. Smaller deletions result in Microdeletion syndrome, which are detected using fluorescence in situ hybridization (FISH) (en)
foaf:depiction
dcterms:subject	Autosomal monosomies and deletions Genetic syndromes
Wikipage page ID	40543679 (xsd:integer)
Wikipage revision ID	1113527912 (xsd:integer)
Link from a Wikipage to another Wikipage	Prader–Willi syndrome FGFRL1 (gene) List of genetic disorders De novo mutation Cri du chat syndrome Genotype Epicanthic fold Gamete LETM1 Autosomal monosomies and deletions Angelman syndrome Deletion (genetics) Microdeletion syndrome Locus (genetics) Genetic syndromes Chromosome Fluorescence in situ hybridization Karyotyping Microcephaly Micrognathia CPLX1 Chromosome 4 (human) Chromosome 5 (human) WHSC1 SLBP Wolf–Hirschhorn syndrome WHSC2 Uniparental disomy Hyperphagia
sameAs	Chromosomal deletion syndrome Chromosomal deletion syndrome Chromosomal deletion syndrome Chromosomal deletion syndrome Chromosomal deletion syndrome
dbp:wikiPageUsesTemplate	dbt:Cn dbt:Infobox_medical_condition_(new) dbt:Reflist
thumbnail	wiki-commons:Special:FilePath/22_del_q11.2.png?width=300
caption	An example of chromosomal deletions (en)
has abstract	Chromosomal deletion syndromes result from deletion of parts of chromosomes. Depending on the location, size, and whom the deletion is inherited from, there are a few known different variations of chromosome deletions. Chromosomal deletion syndromes typically involve larger deletions that are visible using karyotyping techniques. Smaller deletions result in Microdeletion syndrome, which are detected using fluorescence in situ hybridization (FISH) Examples of chromosomal deletion syndromes include 5p-Deletion (cri du chat syndrome), 4p-Deletion (Wolf–Hirschhorn syndrome), Prader–Willi syndrome, and Angelman syndrome. (en)
prov:wasDerivedFrom	wikipedia-en:Chromosomal_deletion_syndrome?oldid=1113527912&ns=0
page length (characters) of wiki page	9094 (xsd:nonNegativeInteger)
foaf:isPrimaryTopicOf	wikipedia-en:Chromosomal_deletion_syndrome
is Link from a Wikipage to another Wikipage of	Deletion (genetics) Microdeletion syndrome List of syndromes Wolf–Hirschhorn syndrome Chromosomal deletion syndromes Chromosome deletion Deletion syndrome
is Wikipage redirect of	Chromosomal deletion syndromes Chromosome deletion Deletion syndrome
is foaf:primaryTopic of	wikipedia-en:Chromosomal_deletion_syndrome

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