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cystinosis

Disease Summary
Associated Targets (2)
Tbio

2


GARD Rare
Mondo Description Cystinosis is a metabolic disease characterized by an accumulation of cystine inside the lysosomes, causing damage in different organs and tissues, particularly in the kidneys and eyes. Three clinical forms have been described: nephropathic infantile, nephropathic juvenile and ocular.
Disease Ontology Description A lysosomal storage disease characterized by the abnormal accumulation of cystine in the lysosomes. It follows an autosomal recessive inheritance pattern and has material basis in mutations in the CTNS gene, located on chromosome 17.
Mondo Term and Equivalent IDs
MONDO:0016239:  cystinosis
GARD:0006236: 
ICD10:E72.04: 
MESH:D003554: 
NCIT:C2976: 
Orphanet:213: 
SCTID:190681003: 
UMLS:C0010690: 
UMLS:CN035091: