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Medical Subject Headings

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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Ciliopathies

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Ciliopathies

Preferred term

Ciliopathies

Topical Descriptor

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.

History note

2017

värekarvojen, siimojen tai ripsien geneettiset häiriöt

Finnish
värekarvoihin, siimoihin tai ripsiin vaikuttavat geneettiset häiriöt
Ciliopatier

Swedish

URI

http://www.yso.fi/onto/mesh/D000072661

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