Congenital chloride diarrhea
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
3
|
55
|
1.000 |
strong |
0.964 |
28 |
55
|
1996 |
2019 |
Ulcerative Colitis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
1458
|
827
|
0.330 |
None |
1.000 |
4 |
1
|
2002 |
2018 |
Diarrhea
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
632
|
63
|
0.200 |
None |
1.000 |
13 |
|
1996 |
2020 |
Dehydration
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
295
|
6
|
0.120 |
None |
1.000 |
2 |
|
2006 |
2010 |
Metabolic alkalosis
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
27
|
5
|
0.110 |
None |
1.000 |
1 |
|
2015 |
2015 |
Alkalosis
|
phenotype |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
25
|
2
|
0.110 |
None |
1.000 |
1 |
|
2019 |
2019 |
Hypochloremia (disorder)
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
7
|
1
|
0.100 |
None |
|
0 |
|
|
|
Serum chloride level decreased (finding)
|
phenotype |
Nutritional and Metabolic Diseases
|
Finding
|
7
|
|
0.100 |
None |
|
0 |
|
|
|
Failure to Thrive
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
842
|
10
|
0.100 |
None |
|
0 |
|
|
|
Hyperactive renin-angiotensin system
|
phenotype |
|
Finding
|
8
|
|
0.100 |
None |
|
0 |
|
|
|
Hyponatremia
|
phenotype |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
109
|
11
|
0.100 |
None |
|
0 |
|
|
|
Hypokalemia
|
phenotype |
Nutritional and Metabolic Diseases
|
Finding
|
61
|
7
|
0.100 |
None |
|
0 |
|
|
|
Hyperaldosteronism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
84
|
6
|
0.100 |
None |
|
0 |
|
|
|
Premature Birth
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
192
|
50
|
0.100 |
None |
|
0 |
|
|
|
Cardiovascular Abnormalities
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
99
|
12
|
0.100 |
None |
|
0 |
|
|
|
Growth delay
|
phenotype |
|
Pathologic Function
|
244
|
40
|
0.100 |
None |
|
0 |
|
|
|
Growth abnormality
|
phenotype |
|
Finding
|
49
|
5
|
0.100 |
None |
|
0 |
|
|
|
Polyhydramnios
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
208
|
28
|
0.100 |
None |
|
0 |
|
|
|
Abdomen distended
|
phenotype |
Digestive System Diseases
|
Finding
|
103
|
6
|
0.100 |
None |
|
0 |
|
|
|
Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
10161
|
1644
|
0.050 |
None |
1.000 |
5 |
|
1998 |
2016 |
Adenoma
|
group |
Neoplasms
|
Neoplastic Process
|
1183
|
103
|
0.050 |
None |
1.000 |
5 |
|
1999 |
2019 |
Central Core Myopathy (disorder)
|
disease |
Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
44
|
110
|
0.040 |
None |
1.000 |
4 |
2
|
2017 |
2019 |
Subfertility, Male
|
phenotype |
Male Urogenital Diseases
|
Sign or Symptom
|
70
|
2
|
0.040 |
None |
1.000 |
4 |
|
2006 |
2017 |
Cleidocranial Dysplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
52
|
22
|
0.040 |
None |
1.000 |
4 |
2
|
2017 |
2019 |
Carcinogenesis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Neoplasms
|
Neoplastic Process
|
6243
|
355
|
0.030 |
None |
1.000 |
3 |
|
1993 |
2002 |