Congenital Disorder

Chromosome Disorders

AMW:DIS:160029

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)

Pathology clinical

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WAGR Syndrome has parent Chromosome Disorders

Rubinstein-Taybi Syndrome has parent Chromosome Disorders

22q11 Deletion Syndrome has parent Chromosome Disorders

Holoprosencephaly has parent Chromosome Disorders

Silver-Russell Syndrome has parent Chromosome Disorders

Angelman Syndrome has parent Chromosome Disorders

Smith-Magenis Syndrome has parent Chromosome Disorders

Cri-du-Chat Syndrome has parent Chromosome Disorders

De Lange Syndrome has parent Chromosome Disorders

Down Syndrome has parent Chromosome Disorders

Prader-Willi Syndrome has parent Chromosome Disorders

Trisomy 13 Syndrome has parent Chromosome Disorders

Williams Syndrome has parent Chromosome Disorders

Trisomy 18 Syndrome has parent Chromosome Disorders

Jacobsen Distal 11q Deletion Syndrome has parent Chromosome Disorders

Beckwith-Wiedemann Syndrome has parent Chromosome Disorders

Branchio-Oto-Renal Syndrome has parent Chromosome Disorders

Sotos Syndrome has parent Chromosome Disorders

Wolf-Hirschhorn Syndrome has parent Chromosome Disorders

Sex Chromosome Disorders has parent Chromosome Disorders

Chromosome Disorders has parent Congenital Abnormalities

Chromosome Disorders has parent Genetic Diseases, Inborn

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