Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 183
Gene Symbol: AGT
AGT
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		0.710 Biomarker GENOMICS_ENGLAND Novel variants detected in AGT gene among patients with essential hypertension. 24452034

2015
Entrez Id: 183
Gene Symbol: AGT
AGT
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		0.710 GermlineCausalMutation ORPHANET Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis. 22095942

2012
Entrez Id: 183
Gene Symbol: AGT
AGT
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		0.710 Biomarker CTD_human A case surviving for over a year of renal tubular dysgenesis with compound heterozygous angiotensinogen gene mutations. 17036344

2006
Entrez Id: 183
Gene Symbol: AGT
AGT
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		0.710 Biomarker CTD_human Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis. 16116425

2005
Entrez Id: 183
Gene Symbol: AGT
AGT
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		0.710 GeneticVariation UNIPROT Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis. 16116425

2005
Entrez Id: 183
Gene Symbol: AGT
AGT
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		0.710 GermlineCausalMutation ORPHANET Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis. 16116425

2005
Entrez Id: 183
Gene Symbol: AGT
AGT
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		0.710 Biomarker GENOMICS_ENGLAND