Cholestasis, benign recurrent intrahepatic 2
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
1
|
11
|
0.720 |
None |
1.000 |
4 |
11
|
2004 |
2016 |
Cholemia
|
disease |
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |
CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3
|
disease |
|
Disease or Syndrome
|
2
|
16
|
0.100 |
None |
|
0 |
3
|
|
|
Obstipation
|
disease |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Cholestasis, progressive familial intrahepatic 3
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
3
|
28
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Cholestasis, benign recurrent intrahepatic 1
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
3
|
9
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Abnormal liver function tests during pregnancy
|
disease |
|
Finding
|
3
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Intermittent jaundice
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Cholestasis, Progressive Familial Intrahepatic, 2
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
4
|
25
|
0.800 |
None |
1.000 |
25 |
24
|
1998 |
2016 |
Low phospholipid-associated cholelithiasis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
5
|
29
|
0.020 |
None |
1.000 |
2 |
2
|
2010 |
2014 |
Cholestasis, chronic
|
disease |
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Intestinal malabsorption of fat
|
phenotype |
Digestive System Diseases; Nutritional and Metabolic Diseases
|
Pathologic Function
|
5
|
|
0.100 |
None |
|
0 |
|
|
|
Congenital hypofibrinogenemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
6
|
10
|
0.300 |
None |
1.000 |
1 |
|
2012 |
2012 |
Afibrinogenemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
9
|
|
0.300 |
None |
1.000 |
1 |
|
2012 |
2012 |
Benign recurrent intrahepatic cholestasis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
10
|
1
|
0.100 |
None |
1.000 |
10 |
1
|
2004 |
2015 |
Chronic hepatitis C genotype 4
|
disease |
|
Disease or Syndrome
|
10
|
3
|
0.010 |
None |
1.000 |
1 |
1
|
2018 |
2018 |
Glucose tolerance test
|
phenotype |
|
Laboratory Procedure
|
17
|
28
|
0.100 |
None |
1.000 |
1 |
1
|
2018 |
2018 |
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
18
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Microvillus inclusion disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
19
|
16
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Neonatal hepatitis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Infections
|
Disease or Syndrome
|
21
|
2
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Death in childhood
|
phenotype |
|
Finding
|
25
|
2
|
0.100 |
None |
|
0 |
|
|
|
Ethylmalonic encephalopathy
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
26
|
33
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Progressive intrahepatic cholestasis (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
31
|
10
|
0.500 |
strong |
1.000 |
61 |
2
|
1997 |
2020 |
Conjugated hyperbilirubinemia
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
32
|
1
|
0.100 |
None |
|
0 |
|
|
|
Acute alcoholic liver disease
|
disease |
Digestive System Diseases; Chemically-Induced Disorders; Mental Disorders
|
Disease or Syndrome
|
35
|
|
0.200 |
None |
1.000 |
1 |
|
2017 |
2017 |