Number of the records: 1
ciliopatie
Record number d000072661 Date 06.06.2025 Type M - MESH Topical term ciliopatie See also (Skutočné meno) dyskinéza ciliárna
UDC C16.131.077.245C16.320.184 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. subject heading
Number of the records: 1