Template:Ciliopathy
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v
t
e
Genetic disorder
, organelle:
Ciliopathy
Structural
receptor:
Polycystic kidney disease
cargo:
Asphyxiating thoracic dysplasia
basal body
:
Bardet–Biedl syndrome
mitotic spindle
:
Meckel syndrome
centrosome
:
Joubert syndrome
Signaling
Nephronophthisis
Other/ungrouped
Alström syndrome
Primary ciliary dyskinesia
Senior–Løken syndrome
Orofaciodigital syndrome 1
McKusick–Kaufman syndrome
Autosomal recessive polycystic kidney
See also:
ciliary proteins
Template:Protein defects by function navs
Categories
:
Navboxes using background colours
Ciliopathy
Genetic disease and disorder templates by mechanism
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