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.