Details for Disease 655

DISEASE NAME Nephronophthisis
DISEASE CATEGORY (ICD10) Congenital malformations, deformations and chromosomal abnormalities
DISEASE ID (ICD10) Q61.5
DISEASE ID (OMIM) 618826; 618697; 617123; 617023; 618613; 613809; 613810; 613827; 613861; 613862; 613983; 614180; 614181; 614494; 614500; 615233; 615434; 615565; 615725; 615780; 617433; 615922; 616188; 616394; 616469; 616544; 616562; 610599; 611131; 612095; 612165; 612572; 612712; 612943; 613194; 613341; 613428; 613464; 613575; 613581; 613582; 613617; 613660; 613731; 613750; 613756; 613758; 613767; 613769; 613794; 613801; 300424; 300605; 312600; 312612; 400004; 600059; 600105; 600132; 600138; 600852; 601414; 601718; 602594; 602772; 604232; 604393; 606068; 607921; 608133; 608380; 609913; 609923; 610282; 610359; 180100; 180104; 180105; 180210; 268000; 268025; 268060; 300029; 300155; 617304; 617460; 618173; 617781; 618220; 618195; 618345; 256100; 602088; 604387; 606966; 611498; 613159; 613820; 613824; 614377; 615382; 615862; 617271
5 combinations linked to 655 OLI211; OLI212; OLI213; OLI214; OLI359
4 gene combinations linked to 655 NPHP1; NPHP3; NPHP3; NPHP4; INVS; NPHP3; CC2D2A; NPHP3; NPHP4
ORPHANET ID 655
Found any issues with the data on this page? Report this entry.