Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 7 of 7 for Ciliopathy
  1. KIF7 gene 
    The KIF7 gene provides instructions for making a protein that is associated with structures called primary cilia. These microscopic, finger-like projections ...
    https://medlineplus.gov/genetics/gene/kif7 - Genetics
  2. NPHP1 gene 
    ... features; such conditions are known as nephronophthisis-associated ciliopathies. Senior-Løken syndrome is characterized by the combination ... likely cause the features of these nephronophthisis-associated ciliopathies, although it remains unclear how these defects lead ...
    https://medlineplus.gov/genetics/gene/nphp1 - Genetics
  3. IFT140 gene 
    ... cilia and involve bone abnormalities are called skeletal ciliopathies. More About This Health Condition MedlinePlus Genetics provides ... V, Rozet JM. Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations. Am J Hum Genet. ...
    https://medlineplus.gov/genetics/gene/ift140 - Genetics
  4. CEP290 gene 
    ... abnormal cilia. These conditions, which are known as ciliopathies, affect many body systems and include Joubert syndrome, ... typically the most severe of the CEP290-associated ciliopathies; affected individuals usually die before or shortly after ...
    https://medlineplus.gov/genetics/gene/cep290 - Genetics
  5. IFT122 gene 
    ... Kuss AW. Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene. Am ...
    https://medlineplus.gov/genetics/gene/ift122 - Genetics
  6. WDR19 gene 
    ... Knappskog PM, Knoers NV, Roepman R, Arts HH. Ciliopathies with skeletal anomalies and renal insufficiency due to ...
    https://medlineplus.gov/genetics/gene/wdr19 - Genetics
  7. WDR35 gene 
    ... WDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype. Am J Med Genet A. ...
    https://medlineplus.gov/genetics/gene/wdr35 - Genetics