Chromosome 10
Chromosome 10
Human chromosome.
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Readers' pathsAug 2026 – Oct 2026
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Apert syndrome
Congenital disorder of the skull and digits.
17%
Chromosome 11
Human chromosome.
15%
Barakat syndrome
Disease characterized by hypoparathyroidism, sensorineural deafness and renal disease.
13%
Cockayne syndrome
Medical condition.
12%
Charcot–Marie–Tooth disease
Neuromuscular disease.
7.4%
Chromosome
DNA molecule containing genetic material of a cell.
6.3%
Usher syndrome
Recessive genetic disorder causing deafblindness.
6.3%
Lysosomal acid lipase deficiency
Medical condition.
6.3%
Hirschsprung's disease
Birth defect in which the intestine lacks certain nerves.
5.3%
Young–Simpson syndrome
Medical condition.
5.3%
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