About: 3q29 microdeletion syndrome

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3q29 microdeletion syndrome is a rare genetic disorder resulting from the deletion of a segment of chromosome 3. This syndrome was first described in 2005.

Attributes	Values
rdf:type	Thing Disease yago:WikicatAutosomalMonosomiesAndDeletions yago:Aberrance114503665 yago:Abnormality114501726 yago:Abstraction100002137 yago:Attribute100024264 yago:ChromosomalAberration114504103 yago:Condition113920835 yago:Disease114070360 yago:IllHealth114052046 yago:Illness114061805 yago:Monosomy114504405 yago:PathologicalState114051917 yago:PhysicalCondition114034177 disease yago:State100024720
rdfs:label	Σύνδρομο μικροδιαγραφής 3q29 (el) 3q29 microdeletion syndrome (en) Síndrome de microdeleción 3q29 (es)
rdfs:comment	3q29 microdeletion syndrome is a rare genetic disorder resulting from the deletion of a segment of chromosome 3. This syndrome was first described in 2005. (en) Το σύνδρομο μικροδιαγραφής 3q29 είναι σπάνια γενετική διαταραχή που προκύπτει από τη διαγραφή ενός τμήματος του χρωμοσώματος 3. Αυτό το σύνδρομο περιγράφηκε για πρώτη φορά το 2005. (el) El síndrome de microdeleción 3q29 es una anomalía genética poco habitual causada por la pérdida o deleción de un segmento del cromosoma 3 humano. Fue descrito por vez primera en el año 2005., lo opuesto de este síndrome es el síndrome de microduplicación 3q29 (es)
foaf:name	3q29 microdeletion syndrome (en)
name	3 (xsd:integer)
foaf:depiction
dcterms:subject	Rare genetic syndromes Syndromes with craniofacial abnormalities Autosomal monosomies and deletions Syndromes with intellectual disability
Wikipage page ID	28203137 (xsd:integer)
Wikipage revision ID	1108497927 (xsd:integer)
Link from a Wikipage to another Wikipage	BDH1 Schizophrenia Melanotransferrin Copy number variant Dysmorphic feature Rare genetic syndromes Syndromes with craniofacial abnormalities Genetic disorder Non-allelic homologous recombination Autosomal monosomies and deletions Deletion (genetics) Autism DLG1 Base pair Chromosome 3 Syndromes with intellectual disability Ataxia Ashkenazi Jews Homology (biology) Phenotype Intellectual disability Microcephaly RING finger domain Nuclear cap-binding protein complex Low copy repeats Philtrum Choline-phosphate cytidylyltransferase Transferrin receptor PAK2
sameAs	3q29 microdeletion syndrome 3q29 microdeletion syndrome 3q29 microdeletion syndrome 3q29 microdeletion syndrome 3q29 microdeletion syndrome 3q29 microdeletion syndrome
dbp:wikiPageUsesTemplate	dbt:Cn dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist dbt:Chromosomal_abnormalities dbt:DECIPHER dbt:Mutation
thumbnail	wiki-commons:Special:FilePath/Human_male_karyotpe_high_resolution_-_Chromosome_3_cropped.png?width=300
ICD	Q93.5 (en)
OMIM	609425 (xsd:integer)
Orphanet	65286 (xsd:integer)
caption	Chromosome 3 is associated with this condition (en)
synonyms	3 (xsd:integer)
has abstract	3q29 microdeletion syndrome is a rare genetic disorder resulting from the deletion of a segment of chromosome 3. This syndrome was first described in 2005. (en) Το σύνδρομο μικροδιαγραφής 3q29 είναι σπάνια γενετική διαταραχή που προκύπτει από τη διαγραφή ενός τμήματος του χρωμοσώματος 3. Αυτό το σύνδρομο περιγράφηκε για πρώτη φορά το 2005. (el) El síndrome de microdeleción 3q29 es una anomalía genética poco habitual causada por la pérdida o deleción de un segmento del cromosoma 3 humano. Fue descrito por vez primera en el año 2005., lo opuesto de este síndrome es el síndrome de microduplicación 3q29 (es)
gold:hypernym	Disorder
prov:wasDerivedFrom	wikipedia-en:3q29_microdeletion_syndrome?oldid=1108497927&ns=0
page length (characters) of wiki page	6824 (xsd:nonNegativeInteger)
ICD10	Q93.5
OMIM id	609425 (xsd:integer)
ORPHA	65286
foaf:isPrimaryTopicOf	wikipedia-en:3q29_microdeletion_syndrome
is Link from a Wikipage to another Wikipage of	FAM43A List of diseases (0–9) Non-allelic homologous recombination Chromosome 3 1q21.1 deletion syndrome List of syndromes
is foaf:primaryTopic of	wikipedia-en:3q29_microdeletion_syndrome

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