REN, renin, 5972

N. diseases: 721; N. variants: 25
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		0.790 CausalMutation disease CLINVAR
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		0.790 Biomarker disease GENOMICS_ENGLAND
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		0.790 Biomarker disease HPO
CUI: C2751310
Disease: Hyperuricemic Nephropathy, Familial Juvenile 2
Hyperuricemic Nephropathy, Familial Juvenile 2 		0.710 Biomarker disease GENOMICS_ENGLAND
CUI: C2751310
Disease: Hyperuricemic Nephropathy, Familial Juvenile 2
Hyperuricemic Nephropathy, Familial Juvenile 2 		0.710 Biomarker disease CTD_human
CUI: C2751310
Disease: Hyperuricemic Nephropathy, Familial Juvenile 2
Hyperuricemic Nephropathy, Familial Juvenile 2 		0.710 CausalMutation disease CLINVAR
CUI: C2751310
Disease: Hyperuricemic Nephropathy, Familial Juvenile 2
Hyperuricemic Nephropathy, Familial Juvenile 2 		0.710 GeneticVariation disease CLINVAR
CUI: C0002871
Disease: Anemia
Anemia 		0.500 Biomarker disease HPO
CUI: C0020649
Disease: Hypotension
Hypotension 		0.400 Biomarker phenotype HPO
CUI: C0027707
Disease: Nephritis, Interstitial
Nephritis, Interstitial 		0.300 Biomarker disease GENOMICS_ENGLAND
CUI: C0041349
Disease: Nephritis, Tubulointerstitial
Nephritis, Tubulointerstitial 		0.300 Biomarker disease GENOMICS_ENGLAND
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		0.200 Biomarker group HPO
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia 		0.170 Biomarker disease HPO
CUI: C0017668
Disease: Focal glomerulosclerosis
Focal glomerulosclerosis 		0.150 Biomarker disease HPO
CUI: C0265783
Disease: Congenital hypoplasia of lung
Congenital hypoplasia of lung 		0.110 Biomarker disease HPO
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis 		0.110 Biomarker phenotype HPO
CUI: C0003460
Disease: Anuria
Anuria 		0.100 Biomarker phenotype HPO
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.100 Biomarker disease HPO
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency 		0.100 Biomarker phenotype HPO
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios 		0.100 Biomarker phenotype HPO
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney 		0.100 Biomarker disease HPO
CUI: C0266619
Disease: Potter's facies
Potter's facies 		0.100 Biomarker disease HPO
CUI: C1849300
Disease: Widely patent fontanelles and sutures
Widely patent fontanelles and sutures 		0.100 Biomarker phenotype HPO
CUI: C1858395
Disease: Tubular atrophy
Tubular atrophy 		0.100 Biomarker phenotype HPO
CUI: C3275899
Disease: Hyperechogenic kidneys
Hyperechogenic kidneys 		0.100 Biomarker phenotype HPO