Ciliopathies (WP4803)
Homo sapiens
The major structures of motile and non-motile cilia (top), the early steps of ciliogenesis (middle), and the links between ciliary trafficking and ciliopathies (bottom) from Reiter 2017.
Authors
Ritchie Lee , Kristina Hanspers , Alex Pico , and Eric WeitzActivity
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Organisms
Homo sapiensCommunities
Rare Diseases Skeletal DysplasiaAnnotations
Disease Ontology
oculocerebrorenal syndrome asphyxiating thoracic dystrophy sensorineural hearing loss Joubert syndrome polycystic kidney disease Meckel syndrome nephronophthisis cone-rod dystrophy primary ciliary dyskinesia infertility holoprosencephaly Senior-Loken syndrome Ellis-Van Creveld syndrome medulloblastoma congenital heart disease juvenile myoclonic epilepsy Leber congenital amaurosis lethal congenital contracture syndrome Pallister-Hall syndrome male infertility retinitis pigmentosa Carpenter syndrome Bardet-Biedl syndrome hydrolethalus syndrome Greig cephalopolysyndactyly syndrome Birt-Hogg-Dube syndrome orofaciodigital syndrome ciliopathyPathway Ontology
disease pathwayReferences
- Genes and molecular pathways underpinning ciliopathies. Reiter JF, Leroux MR. Nat Rev Mol Cell Biol. 2017 Sep;18(9):533–47. PubMed Europe PMC Scholia