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Cockayne Syndrome

"Cockayne Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

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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".

Diseases [C]
Musculoskeletal Diseases [C05]
Bone Diseases [C05.116]
Bone Diseases, Developmental [C05.116.099]
Dwarfism [C05.116.099.343]
Cockayne Syndrome [C05.116.099.343.250]
Nervous System Diseases [C10]
Neurodegenerative Diseases [C10.574]
Heredodegenerative Disorders, Nervous System [C10.574.500]
Cockayne Syndrome [C10.574.500.362]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
Cockayne Syndrome [C16.131.077.250]
Genetic Diseases, Inborn [C16.320]
Dwarfism [C16.320.240]
Cockayne Syndrome [C16.320.240.562]
Heredodegenerative Disorders, Nervous System [C16.320.400]
Cockayne Syndrome [C16.320.400.200]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
DNA Repair-Deficiency Disorders [C18.452.284]
Cockayne Syndrome [C18.452.284.250]

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

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

Publications

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This graph shows the total number of publications written about "Cockayne Syndrome" by people in this website by year, and whether "Cockayne Syndrome" was a major or minor topic of these publications.

Bar chart showing 1 publications over 1 distinct years, with a maximum of 1 publications in 2018

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2018	0	1	1

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Cockayne Syndrome