Ciliopathies

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.

Year introduced: 2017

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C16.131.077.245, C16.320.184

MeSH Unique ID: D000072661

Entry Terms:

• Ciliopathy

Previous Indexing:

• Cilia (2007-2016)
• Ciliary Motility Disorders (2009-2016)

See Also:

• Ciliary Motility Disorders

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Ciliopathies
Alstrom Syndrome
Bardet-Biedl Syndrome
Caroli Disease
Ciliary Motility Disorders
Kartagener Syndrome
von Hippel-Lindau Disease

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Ciliopathies
Alstrom Syndrome
Bardet-Biedl Syndrome
Caroli Disease
Ciliary Motility Disorders
Kartagener Syndrome
Polycystic Kidney Diseases
Polycystic Kidney, Autosomal Dominant
Polycystic Kidney, Autosomal Recessive
von Hippel-Lindau Disease