×
Entrez Id:
3145
Gene Symbol:
HMBS
HMBS
0.100
CausalMutation
phenotype
CLINVAR
×
Entrez Id:
1181
Gene Symbol:
CLCN2
CLCN2
0.100
CausalMutation
phenotype
CLINVAR
×
Entrez Id:
2908
Gene Symbol:
NR3C1
NR3C1
0.400
Biomarker
phenotype
CTD_human
Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene.
11932321
2002
×
Entrez Id:
154
Gene Symbol:
ADRB2
ADRB2
0.310
Biomarker
phenotype
CTD_human
Debrisoquine phenotype and the pharmacokinetics and beta-2 receptor pharmacodynamics of metoprolol and its enantiomers.
1848636
1991
×
Entrez Id:
154
Gene Symbol:
ADRB2
ADRB2
0.310
Biomarker
phenotype
CTD_human
The influence of the AA 16 beta 2-adrenoceptor polymorphism on systemic and airway responses in asthma.
17292646
2008
×
Entrez Id:
154
Gene Symbol:
ADRB2
ADRB2
0.310
Biomarker
phenotype
CTD_human
Beta-2-adrenoceptor-mediated hypokalemia and its abolishment by oxprenolol.
2826064
1987
×
Entrez Id:
5443
Gene Symbol:
POMC
POMC
0.300
Biomarker
phenotype
CTD_human
Adrenocorticotrophin-induced hypertension: effects of mineralocorticoid and glucocorticoid receptor antagonism.
10100081
1999
×
Entrez Id:
183
Gene Symbol:
AGT
AGT
0.300
Therapeutic
phenotype
CTD_human
Factitious Bartter's syndrome induced by surreptitious intake of furosemide.
7182184
1982
×
Entrez Id:
5443
Gene Symbol:
POMC
POMC
0.300
Biomarker
phenotype
CTD_human
Chronic potentiation of vasoconstrictor hypertension by adrenocorticotropic hormone.
6279499
1982
×
Entrez Id:
5443
Gene Symbol:
POMC
POMC
0.300
Biomarker
phenotype
CTD_human
[Treatment of infantile spasms with long-term low dose ACTH].
1327015
1992
×
Entrez Id:
5443
Gene Symbol:
POMC
POMC
0.300
Biomarker
phenotype
CTD_human
ACTH therapy in infantile spasms: side effects.
6254450
1980
×
Entrez Id:
5443
Gene Symbol:
POMC
POMC
0.300
Biomarker
phenotype
CTD_human
Mineralocorticoid hypertension in childhood.
323586
1977
×
Entrez Id:
5443
Gene Symbol:
POMC
POMC
0.300
Biomarker
phenotype
CTD_human
Colonic adenocarcinoma associated ectopic ACTH secretion: a case history.
8562174
1995
×
Entrez Id:
4879
Gene Symbol:
NPPB
NPPB
0.300
Biomarker
phenotype
CTD_human
Low-dose nesiritide improves renal function in heart failure patients following acute myocardial infarction.
20339970
2010
×
Entrez Id:
5443
Gene Symbol:
POMC
POMC
0.300
Biomarker
phenotype
CTD_human
Treatment of ocular myasthenia with corticotrophin.
4323972
1971
×
Entrez Id:
5443
Gene Symbol:
POMC
POMC
0.300
Biomarker
phenotype
CTD_human
ACTH revisited: effective treatment for acute crystal induced synovitis in patients with multiple medical problems.
8035395
1994
×
Entrez Id:
5443
Gene Symbol:
POMC
POMC
0.300
Biomarker
phenotype
CTD_human
Syndrome of inappropriate ADH secretion concealed by hypokalaemia due to ectopic ACTH production.
6258369
1981
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.300
Biomarker
phenotype
CTD_human
Insulin-induced weakness in hypokalemic myopathy.
496411
1979
×
Entrez Id:
6750
Gene Symbol:
SST
SST
0.300
Therapeutic
phenotype
CTD_human
Effects of somatostatin and oral potassium administration on terbutaline-induced hypokalemia.
2563217
1989
×
Entrez Id:
154
Gene Symbol:
ADRB2
ADRB2
0.310
GeneticVariation
phenotype
LHGDN
The influence of the AA 16 beta 2-adrenoceptor polymorphism on systemic and airway responses in asthma.
17292646
2008
×
Entrez Id:
115111
Gene Symbol:
SLC26A7
SLC26A7
0.010
AlteredExpression
phenotype
LHGDN
Chloride/bicarbonate exchanger SLC26A7 is localized in endosomes in medullary collecting duct cells and is targeted to the basolateral membrane in hypertonicity and potassium depletion .
16524946
2006
×
Entrez Id:
2908
Gene Symbol:
NR3C1
NR3C1
0.400
Biomarker
phenotype
HPO
×
Entrez Id:
657
Gene Symbol:
BMPR1A
BMPR1A
0.100
Biomarker
phenotype
HPO
×
Entrez Id:
1586
Gene Symbol:
CYP17A1
CYP17A1
0.100
Biomarker
phenotype
HPO
×
Entrez Id:
6340
Gene Symbol:
SCNN1G
SCNN1G
0.100
Biomarker
phenotype
HPO