: MeSH: Ciliopathies

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

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

Ciliopathies

Notice: Undefined index: in /var/www/html/model/Concept.php on line 545

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.

http://data.loterre.fr/ark:/67375/JVR-R7P0HLSM-3

RDF/XML TURTLE JSON-LD Creado 5/7/16, última modificación 14/12/17

Loterre