Condition: Allanson Pantzar McLeod syndrome


rs797045079 in ACE gene and Allanson Pantzar McLeod syndrome PMID 22095942 2012 Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis.

rs74315283 in AGT gene and Allanson Pantzar McLeod syndrome PMID 16116425 2005 Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis.

rs104893677 in AGTR1 gene and Allanson Pantzar McLeod syndrome PMID 16116425 2005 Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis.

rs1135401743 in HAAO;MTA3 gene and Allanson Pantzar McLeod syndrome PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs75462234 in PAX2 gene and Allanson Pantzar McLeod syndrome PMID 27657687 2017 Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.

rs121917742 in REN gene and Allanson Pantzar McLeod syndrome PMID 16116425 2005 Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis.