A syndrome characterized by multiple system abnormalities including DWARFISM; PHOTOSENSITIVITY DISORDERS; PREMATURE AGING; and HEARING LOSS. It is caused by mutations of a number of autosomal recessive genes encoding proteins that involve transcriptional-coupled DNA REPAIR processes. Cockayne syndrome is classified by the severity and age of onset. Type I (classical; CSA) is early childhood onset in the second year of life; type II (congenital; CSB) is early onset at birth with severe symptoms; type III (xeroderma pigmentosum; XP) is late childhood onset with mild symptoms.

Descriptor ID	D003057
MeSH Number(s)	C05.116.099.343.250 C10.574.500.362 C16.131.077.250 C16.320.240.562 C16.320.400.200 C18.452.284.250
Concept/Terms	Cockayne Syndrome Cockayne Syndrome Syndrome, Cockayne Progeria-Like Syndrome Progeria Like Syndrome Progeria-Like Syndromes Syndrome, Progeria-Like Progeroid Nanism Dwarfism-Retinal Atrophy-Deafness Syndrome Cockayne Syndrome, Type II Cockayne Syndrome, Type II Type II Cockayne Syndrome Group B Cockayne Syndrome Type B Cockayne Syndrome Cockayne Syndrome, Group B Cockayne Syndrome, Type B Cockayne Syndrome, Type III Cockayne Syndrome, Type III Cockayne Syndrome Type C Type III Cockayne Syndrome Cockayne Syndrome, Type C Group C Cockayne Syndrome Type C Cockayne Syndrome Cockayne Syndrome Type 3 Cockayne Syndrome, Group C Cockayne Syndrome, Type I Cockayne Syndrome, Type I Type I Cockayne Syndrome Group A Cockayne Syndrome Type A Cockayne Syndrome Cockayne Syndrome, Group A Cockayne Syndrome, Type A

Below are MeSH descriptors whose meaning is more general than "Cockayne Syndrome".

Below are MeSH descriptors whose meaning is related to "Cockayne Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Cockayne Syndrome".