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Ciliopathies MeSH Descriptor Data 2021


MeSH Heading
Ciliopathies
Tree Number(s)
C16.131.077.245
C16.320.184
Unique ID
D000072661
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000072661
Scope Note
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.
Previous Indexing
Cilia (2007-2016)
Ciliary Motility Disorders (2009-2016)
See Also
Ciliary Motility Disorders
Public MeSH Note
2017
History Note
2017
Date Established
2017/01/01
Date of Entry
2016/07/05
Revision Date
2017/12/14
Ciliopathies Preferred
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