Structured Summary
Abstract
Genetic disorders caused by defects in genes related to the primary CILIUM; BASAL BODY; or CENTROSOME. Primary features may include obesity, SKELETAL DYSPLASIA; POLYDACTYLY and malformations that primarily involve the liver, eye or kidneys.
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Classification
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Synonyms
1 entry terms
- Ciliopathy
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2017
MeSH Record
Previous Indexing
- Cilia (2007-2016)
- Ciliary Motility Disorders (2009-2016)
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AMA Style
References
- National Library of Medicine. Ciliopathies. Medical Subject Headings (MeSH). 2026. Unique ID D000072661. http://id.nlm.nih.gov/mesh/2026/D000072661
- Ciliopathies. In: Wikipedia. https://en.wikipedia.org/wiki/Ciliopathy
- Ciliopathies. In: Wikidata. https://www.wikidata.org/wiki/Q203031