Chromosome Disorders

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)

Year introduced: 2002

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Subheadings:

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C16.131.260, C16.320.180

MeSH Unique ID: D025063

Entry Terms:

• Chromosome Disorder
• Disorder, Chromosome
• Disorders, Chromosome
• Chromosome Abnormality Disorders
• Chromosome Abnormality Disorder
• Disorder, Chromosome Abnormality
• Chromosomal Disorders
• Chromosomal Disorder
• Disorder, Chromosomal
• Disorders, Chromosomal
• Autosomal Chromosome Disorders
• Autosomal Chromosome Disorder
• Chromosome Disorder, Autosomal
• Chromosome Disorders, Autosomal

Previous Indexing:

• Chromosome Abnormalities (1964-2001)

See Also:

• Cytogenetics
• Genetics, Medical

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
22q11 Deletion Syndrome
DiGeorge 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
Fragile X Syndrome
Orofaciodigital Syndromes
Sex Chromosome Disorders of Sex Development +
Silver-Russell Syndrome
Smith-Magenis Syndrome
Sotos Syndrome
Trisomy 13 Syndrome
Trisomy 18 Syndrome
WAGR Syndrome
Williams Syndrome
Wolf-Hirschhorn Syndrome

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Chromosome Disorders
22q11 Deletion Syndrome
DiGeorge 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
Fragile X Syndrome
Orofaciodigital Syndromes
Sex Chromosome Disorders of Sex Development +
Silver-Russell Syndrome
Smith-Magenis Syndrome
Sotos Syndrome
Trisomy 13 Syndrome
Trisomy 18 Syndrome
WAGR Syndrome
Williams Syndrome
Wolf-Hirschhorn Syndrome