Congenital Disorder

Ciliopathies

AMW:DIS:160008

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.

Pathology clinical

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Ciliopathies has parent Abnormalities, Multiple

Caroli Disease has parent Ciliopathies

Ciliary Motility Disorders has parent Ciliopathies

Bardet-Biedl Syndrome has parent Ciliopathies

Alstrom Syndrome has parent Ciliopathies

von Hippel-Lindau Disease has parent Ciliopathies

Polycystic Kidney Diseases has parent Ciliopathies

Ciliopathies has parent Genetic Diseases, Inborn

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