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Up to: Autosomal recessive disease · Cystinosis
Nephropathic cystinosis
An autosomal recessive condition caused by mutation(s) in the CTNS gene, encoding cystinosin. It is a sub-type of cystinosis, in which accumulation of cystine in the kidney results in renal dysfunction.
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Juvenile nephropathic cystinosis 0 trials
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Nephropathic infantile cystinosis 0 trials