Pseudohypoaldosteronism, Type IIb
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
2
|
8
|
0.700 |
strong |
1.000 |
4 |
8
|
2001 |
2013 |
Hypertensive disease
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
2322
|
1085
|
0.500 |
None |
0.909 |
44 |
2
|
2003 |
2020 |
Pseudohypoaldosteronism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
19
|
3
|
0.410 |
None |
1.000 |
2 |
|
2012 |
2013 |
Pseudohypoaldosteronism, Type II
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
27
|
42
|
0.400 |
None |
0.976 |
42 |
1
|
2003 |
2020 |
Schizophrenia
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
2872
|
2897
|
0.310 |
None |
< 0.001 |
1 |
|
2011 |
2011 |
Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Respiratory Tract Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
2
|
1
|
0.300 |
strong |
1.000 |
1 |
|
2008 |
2008 |
Hyperpotassemia and Hypertension, Familial
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
10
|
|
0.300 |
None |
1.000 |
1 |
|
2012 |
2012 |
Pseudohypoaldosteronism, Type I
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
19
|
|
0.300 |
None |
1.000 |
1 |
|
2012 |
2012 |
Pseudohypoaldosteronism, Type I, Autosomal Recessive
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
10
|
6
|
0.300 |
None |
1.000 |
1 |
|
2012 |
2012 |
Pseudohypoaldosteronism, Type I, Autosomal Dominant
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
13
|
20
|
0.300 |
None |
1.000 |
1 |
|
2012 |
2012 |
Ovarian Mucinous Adenocarcinoma
|
disease |
Neoplasms
|
Neoplastic Process
|
45
|
24
|
0.300 |
None |
|
0 |
|
|
|
Metastatic melanoma
|
disease |
Neoplasms
|
Neoplastic Process
|
504
|
42
|
0.300 |
None |
|
0 |
|
|
|
Gitelman Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
26
|
120
|
0.200 |
None |
1.000 |
1 |
|
2012 |
2012 |
Transient Ischemic Attack
|
disease |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
344
|
16
|
0.200 |
None |
1.000 |
1 |
|
2017 |
2017 |
Hyperkalemia
|
phenotype |
Nutritional and Metabolic Diseases
|
Finding
|
32
|
1
|
0.110 |
None |
1.000 |
1 |
|
2004 |
2004 |
Hyperkalemic Mineralocorticoid Resistance
|
disease |
|
Disease or Syndrome
|
22
|
3
|
0.100 |
None |
0.976 |
42 |
1
|
2003 |
2020 |
Essential Hypertension
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
445
|
293
|
0.100 |
None |
0.800 |
10 |
|
2003 |
2016 |
Hyperchloremia
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
12
|
2
|
0.100 |
None |
|
0 |
|
|
|
Hyperchloremic metabolic acidosis
|
phenotype |
|
Disease or Syndrome
|
8
|
|
0.100 |
None |
|
0 |
|
|
|
PSEUDOHYPOALDOSTERONISM, TYPE IID
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
13
|
29
|
0.090 |
None |
1.000 |
9 |
|
2007 |
2018 |
ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
|
Disease or Syndrome
|
15
|
3
|
0.060 |
None |
1.000 |
6 |
|
2004 |
2015 |
genetic hypertension
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
34
|
2
|
0.030 |
None |
1.000 |
3 |
|
2004 |
2011 |
Hypocalciuric hypercalcemia, familial, type 1
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
46
|
58
|
0.020 |
None |
1.000 |
2 |
2
|
2007 |
2007 |
Hypercalciuria
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
60
|
5
|
0.020 |
None |
1.000 |
2 |
|
2004 |
2007 |
Influenza A
|
disease |
|
Disease or Syndrome
|
563
|
19
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |