5 genes annotated in human
An autosomal recessive genetic disease characterized by progressive wasting of the filtering unit of the kidney (nephronophthisis), with or without medullary cystic renal disease, and progressive eye disease.
In addition to gene-name show these genes:
Click on a gene's description to view its network relationships with genes known to be involved in "senior loken syndrome"
|Name||Description||Probability||Func Analog Organism|
|NPHP1||nephronophthisis 1 (juvenile)||0.001|
|SDCCAG8||serologically defined colon cancer antigen 8||0.001|
|CEP290||centrosomal protein 290kDa||0.001|
|IQCB1||IQ motif containing B1||0.000|