Finnish congenital nephrotic syndrome

Disease Term Disease ID Gene Symbol Classification References Source
Finnish congenital nephrotic syndrome C0403399 ALG1 Causal Pathogenic evidence from ClinVar - ClinVar
NPHS1 Causal Pathogenic evidence from ClinVar 9660941, 9915943, 10577936, 10652016, 10792613, 10972661, 11012881, 11317351, 11562357, 11726550, 11854170, 14570703, 15086927, 15213260, 15338398, 15780077, 15906409, 16316524, 16518627, 17290294, 17371932, 18503012, 18614772, 18709391, 19194555, 19321760, 19406966, 19423745, 19812541, 20172850, 20507940, 20798252, 21415313, 21672106, 22009864, 22099579, 22565185, 22584503, 22732337, 23595123, 23949594, 24142548, 24303155, 24498843, 24742477, 24902943, 25349199, 25407002, 25501161, 25525159, 25720465, 25729976, 25804400, 26560236, 26668027, 27019444, 28117080, 28204945, 28392951, 28780565, 29474669 ClinVar
TTC21B Causal Pathogenic evidence from ClinVar - ClinVar
TTC21B-AS1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -