NPHS1, NPHS1 adhesion molecule, nephrin, 4868

N. diseases: 87; N. variants: 189
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0403399
Disease: Finnish congenital nephrotic syndrome
Finnish congenital nephrotic syndrome 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C3501848
Disease: Nephrosis, congenital
Nephrosis, congenital 		0.500 GeneticVariation disease CLINVAR
CUI: C3501848
Disease: Nephrosis, congenital
Nephrosis, congenital 		0.500 Biomarker disease HPO
CUI: C0033687
Disease: Proteinuria
Proteinuria 		0.410 CausalMutation phenotype CLINVAR
CUI: C0033687
Disease: Proteinuria
Proteinuria 		0.410 Biomarker phenotype HPO
CUI: C0017658
Disease: Glomerulonephritis
Glomerulonephritis 		0.400 Biomarker disease HPO
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		0.400 Biomarker group MGD
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		0.400 Biomarker group HPO
CUI: C0268731
Disease: Renal glomerular disease
Renal glomerular disease 		0.300 Biomarker group GENOMICS_ENGLAND
CUI: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment 		0.300 Biomarker phenotype GENOMICS_ENGLAND
CUI: C0403397
Disease: Steroid-resistant nephrotic syndrome
Steroid-resistant nephrotic syndrome 		0.200 GeneticVariation disease CLINVAR
CUI: C0178664
Disease: Glomerulosclerosis (disorder)
Glomerulosclerosis (disorder) 		0.120 Biomarker disease HPO
CUI: C0011991
Disease: Diarrhea
Diarrhea 		0.110 CausalMutation phenotype CLINVAR
CUI: C0239981
Disease: Hypoalbuminemia
Hypoalbuminemia 		0.110 Biomarker disease HPO
CUI: C0268747
Disease: Diffuse mesangial sclerosis (disorder)
Diffuse mesangial sclerosis (disorder) 		0.110 Biomarker disease HPO
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency 		0.110 Biomarker disease HPO
CUI: C0000731
Disease: Abdomen distended
Abdomen distended 		0.100 Biomarker phenotype HPO
CUI: C0003962
Disease: Ascites
Ascites 		0.100 CausalMutation phenotype CLINVAR
CUI: C0013604
Disease: Edema
Edema 		0.100 CausalMutation phenotype CLINVAR
CUI: C0013604
Disease: Edema
Edema 		0.100 Biomarker phenotype HPO
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		0.100 Biomarker disease HPO
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia 		0.100 Biomarker disease HPO
CUI: C0020639
Disease: Hypoproteinemia
Hypoproteinemia 		0.100 Biomarker disease HPO
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.100 Biomarker disease HPO
CUI: C0032285
Disease: Pneumonia
Pneumonia 		0.100 CausalMutation disease CLINVAR