Disease_Mapped_To_Gene
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.
C129932
C2931187
Cellosaurus
Disease or Syndrome
Nephropathic Cystinosis
Nephropathic Cystinosis
Cellosaurus Disease Terminology
CTNS Gene
Cellosaurus Terminology
Cystinosis