Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 Biomarker phenotype BEFREE Central diabetes insipidus (CDI) is characterized by polyuria and polydipsia caused by impairment of arginine vasopressin (AVP) secretion. 31748430 2020
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 Biomarker phenotype BEFREE Alternatively, hypoarousal could be a side effect of diabetes insipidus - polydipsia and polyuria seen in Hom rats due to loss of AVP facilitation of water reabsorption in the kidney. 31160697 2019
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 Biomarker phenotype BEFREE Absence of the anti-diuretic hormone, arginine vasopressin (AVP), facilitates copious free water urinary excretion (polyuria) in equal volumes to polydipsia to maintain plasma tonicity within normal physiological limits. 31284689 2019
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 GeneticVariation phenotype BEFREE Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI) is characterized by severe polyuria and polydipsia and is caused by variations in the gene encoding the AVP prohormone. 29949799 2018
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 Biomarker phenotype BEFREE Diabetes insipidus is a disease characterized by polyuria and polydipsia due to inadequate release of arginine vasopressin from the posterior pituitary gland (neurohypophyseal diabetes insipidus) or due to arginine vasopressin insensitivity by the renal distal tubule, leading to a deficiency in tubular water reabsorption (nephrogenic diabetes insipidus). 28476225 2017
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 GeneticVariation phenotype BEFREE Neurohypophyseal diabetes insipidus is characterized by polyuria and polydipsia owing to partial or complete deficiency of the antidiuretic hormone, arginine vasopressin (AVP). 27156762 2016
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 Biomarker phenotype BEFREE Familial neurohypophyseal diabetes insipidus (FNDI) is a rare hereditary disorder with unknown prevalence characterized by arginine-vasopressin hormone (AVP) deficiency resulting in polyuria and polydipsia from early childhood. 27539621 2016
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 GeneticVariation phenotype BEFREE Familial neurohypophyseal diabetes insipidus (FNDI) is a genetic disorder presenting with polyuria and polydipsia and is caused by mutations in the arginine vasopressin-neurophysin II (AVP-NPII) gene. 27513365 2016
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 Biomarker phenotype BEFREE The mutations lead to aberrant preprohormone processing and progressive destruction of AVP-secreting cells, which gradually manifests a progressive polyuria and polydipsia during early childhood, and a disorder of water homeostasis. 23252994 2013
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 Biomarker phenotype BEFREE Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI) is a rare autosomal dominant disorder characterized by polyuria and polydipsia due to deficiency of arginine vasopressin (AVP). 19169480 2008
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 Biomarker phenotype BEFREE Congenital nephrogenic diabetes insipidus (NDI) is a chronic disorder involving polyuria and polydipsia that results from unresponsiveness of the renal collecting ducts to the antidiuretic hormone vasopressin. 18653713 2008
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 GeneticVariation phenotype BEFREE The homozygous individuals reported subjective improvement in polyuria and polydipsia with the use of dDAVP (1-desamino-8-D-arginine-vasopressin). 15100362 2004
Entrez Id: 551
Gene Symbol: AVP
AVP
0.200 Biomarker phenotype HPO