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nephronophthisis 18

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any nephronophthisis in which the cause of the disease is a mutation in the CEP83 gene.
Uniprot Description An autosomal recessive disorder characterized by chronic tubulointerstitial nephritis resulting in end-stage renal disease in early childhood. Extrarenal manifestations, including intellectual disability or liver changes, may occur in some patients.
Disease Ontology Description A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the CEP83 gene on chromosome 12q22.
Mondo Term and Equivalent IDs
MONDO:0014374:  nephronophthisis 18
UMLS:C3890591: