Mesh term Chromosome Disorders
Browse to parent terms:Congenital Abnormalities
Genetic Diseases, Inborn
Description
Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material (either a whole chromosome or a chromosome segment). (from Thompson et al., Genetics in Medicine, 5th ed, p429)Browse to child terms:
22q11 Deletion Syndrome
Angelman Syndrome
Beckwith-Wiedemann Syndrome
Branchio-Oto-Renal Syndrome
Cri-du-Chat Syndrome
De Lange Syndrome
Down Syndrome
Holoprosencephaly
Jacobsen Distal 11q Deletion Syndrome
Prader-Willi Syndrome
Rubinstein-Taybi Syndrome
Sex Chromosome Disorders
Silver-Russell Syndrome
Smith-Magenis Syndrome
Sotos Syndrome
Trisomy 13 Syndrome
Trisomy 18 Syndrome
WAGR Syndrome
Williams Syndrome
Wolf-Hirschhorn Syndrome
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