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Chromosomes, Human, Pair 13

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Definition: A specific pair of GROUP D CHROMOSOMES of the human chromosome classification.      Other names Chromosome 13
 
SubstanceCAS Registry & nameCategoriesSource
Chromosome 13 ring  0   *Ring Chromosomes Chromosomes, Human, Pair 13.
Uniparental disomy of 13  0   *Uniparental Disomy Chromosomes, Human, Pair 13.
Patau syndrome  0   *Trisomy *Chromosome Disorders Chromosomes, Human, Pair 13.
Pseudotrisomy 13 syndrome  0   *Fetal Macrosomia *Hand Deformities, Congenital *Trisomy *Holoprosencephaly *Polydactyly Chromosomes, Human, Pair 13.
Chromosome 13q-mosaicism  0   *Chromosome Disorders Chromosomes, Human, Pair 13 Mosaicism.
Chromosome 13q trisomy  0   *Trisomy Chromosomes, Human, Pair 13.
13q deletion syndrome  0   *Chromosome Deletion *Chromosome Disorders Chromosomes, Human, Pair 13.
Chromosome 13p duplication  0   *Trisomy Chromosomes, Human, Pair 13.
Deletion 13q syndrome, partial  0   *Chromosome Deletion *Chromosome Disorders Chromosomes, Human, Pair 13.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012
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