Trisomy 13 SyndromeTrisomy 18 SyndromeBeckwith-Wiedemann SyndromeCri-du-Chat SyndromeDe Lange SyndromeDown SyndromePrader-Willi SyndromeRubinstein-Taybi SyndromeHoloprosencephalyAngelman SyndromeWAGR SyndromeWilliams SyndromeBranchio-Oto-Renal SyndromeSex Chromosome DisordersJacobsen Distal 11q Deletion SyndromeWolf-Hirschhorn SyndromeSilver-Russell Syndrome22q11 Deletion SyndromeSotos SyndromeSmith-Magenis Syndrome
broaderDescriptor
Chromosome Disorders/diagnostic imagingChromosome Disorders/bloodChromosome Disorders/cerebrospinal fluidChromosome Disorders/chemically inducedChromosome Disorders/classificationChromosome Disorders/complicationsChromosome Disorders/diagnosisChromosome Disorders/diet therapyChromosome Disorders/drug therapyChromosome Disorders/economicsChromosome Disorders/embryologyChromosome Disorders/enzymologyChromosome Disorders/ethnologyChromosome Disorders/etiologyChromosome Disorders/geneticsChromosome Disorders/historyChromosome Disorders/immunologyChromosome Disorders/metabolismChromosome Disorders/microbiologyChromosome Disorders/mortalityChromosome Disorders/nursingChromosome Disorders/epidemiologyChromosome Disorders/parasitologyChromosome Disorders/pathologyChromosome Disorders/physiopathologyChromosome Disorders/prevention & controlChromosome Disorders/psychologyChromosome Disorders/radiotherapyChromosome Disorders/rehabilitationChromosome Disorders/surgeryChromosome Disorders/therapyChromosome Disorders/urineChromosome Disorders/veterinaryChromosome Disorders/virology
hasDescriptor
Recombinant chromosome 8 syndromeChromosome 1p36 Deletion SyndromeDeletion 13q syndrome, partial13q deletion syndromeChromosome 13q-mosaicismEmanuel syndromeSchmid-Fraccaro syndromeThrombocytopenia chromosome breakageChromosome 18 deletion syndromeWarburton Anyane Yeboa syndromeTrisomy 22 mosaicism syndromeChromosome 22, monosome mosaicTelomeric 22q13 Monosomy SyndromeChromosome 3 duplication syndromeMosaic variegated aneuploidy syndromePartial Trisomy 3q SyndromeRing chromosome 4 syndromeChromosome 4q- SyndromeChromosome 4, 4q Terminal Deletion SyndromeDuplication 4p SyndromeChromosome 6 ring syndromeChromosome 10q duplication syndrome6q+ Syndrome, PartialChromosome 7 ring syndrome7p2 monosomy syndromePartial Duplication 15q SyndromeDistal Trisomy 10q SyndromePallister Killian syndrome10p Deletion Syndrome (Partial)Chromosome 18p deletion syndromePotocki-Lupski syndromePotocki-Shaffer syndromeEdinburgh Malformation SyndromeTrisomy 18-Like SyndromeOtodental DysplasiaContiguous Abcd1-Dxs1375e Deletion SyndromeFragile Site 16p12Delayed Cranial Ossification due to CBFB HaploinsufficiencyMonosomy 7 of Bone MarrowMental Retardation, Fra12a Type
preferredMappedTo
allowableQualifier
annotation
GEN or unspecified; prefer specifics; coord IM with specific numbered chromosome (IM)
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broaderDescriptor
dateCreated
2001-07-25
dateEstablished
2002-01-01
dateRevised
2009-07-06
historyNote
2002; see CHROMOSOMAL ABNORMALITIES 1978-1995
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identifier
preferredConcept
preferredTerm
previousIndexing
Chromosome Abnormalities (1964-2001)
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publicMeSHNote
2002
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treeNumber
label
Chromosome Disorders
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