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Ontology Term : Senior-Loken syndrome UniProtKeyword

description  Protein which, if defective, causes Senior-Loken syndrome, a genetically and clinically heterogeneous disease characterized by nephronophthisis and retinal abnormalities manifesting as congenital retinal blindness or retinitis pigmentosa. Senior-Loken syndrome can be associated with manifestations such as cerebellar ataxia and skeletal abnormalities including cone epiphyses
  • synonyms:
  • Loken-Senior syndrome,
  • Renal dysplasia and retinal aplasia,
  • Renal-retinal syndrome,
  • Senior-Loeken syndrome,
  • Juvenile nephronophthisis with Leber amaurosis
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