CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1
|
disease |
|
Disease or Syndrome
|
1
|
4
|
0.600 |
None |
1.000 |
4 |
4
|
2005 |
2016 |
Red Blood Cell Count measurement
|
phenotype |
|
Laboratory Procedure
|
717
|
1599
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Cholestasis, chronic
|
disease |
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Post surgical diarrhea
|
phenotype |
|
Sign or Symptom
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Serum gamma-glutamyl transferase measurement
|
phenotype |
|
Laboratory Procedure
|
54
|
108
|
0.100 |
None |
1.000 |
1 |
1
|
2011 |
2011 |
Familial (FPAH)
|
disease |
|
Disease or Syndrome
|
1075
|
276
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
|
disease |
|
Finding
|
578
|
1158
|
0.100 |
None |
1.000 |
1 |
1
|
2018 |
2018 |
Elevated hepatic transaminase
|
phenotype |
|
Finding
|
212
|
9
|
0.100 |
None |
|
0 |
|
|
|
Increased serum bile acid concentration during pregnancy
|
phenotype |
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormal liver function tests during pregnancy
|
disease |
|
Finding
|
3
|
1
|
0.100 |
None |
|
0 |
|
|
|
Increased serum bile acid concentration
|
phenotype |
|
Finding
|
5
|
|
0.100 |
None |
|
0 |
|
|
|
Multiple congenital anomalies
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
251
|
350
|
0.100 |
None |
1.000 |
6 |
1
|
1998 |
2015 |
Alagille Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
Congenital Abnormality
|
38
|
18
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
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 |
|
1997 |
1997 |
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 |
0.929 |
14 |
|
1997 |
2015 |
Cystic Fibrosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases
|
Disease or Syndrome
|
852
|
704
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |
Dwarfism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
1261
|
77
|
0.110 |
None |
1.000 |
1 |
|
2003 |
2003 |
Acute Chest Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
405
|
135
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Cholestasis, progressive familial intrahepatic 1
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
38
|
19
|
0.800 |
None |
0.978 |
45 |
13
|
1996 |
2018 |
Cholestasis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
420
|
15
|
0.100 |
None |
0.958 |
24 |
|
1998 |
2019 |
Intrahepatic Cholestasis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
54
|
3
|
0.480 |
None |
1.000 |
9 |
|
2001 |
2017 |
Liver diseases
|
group |
Digestive System Diseases
|
Disease or Syndrome
|
1019
|
100
|
0.080 |
None |
1.000 |
8 |
|
2003 |
2017 |
Cholestasis, benign recurrent intrahepatic 1
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
3
|
9
|
0.700 |
None |
1.000 |
5 |
9
|
1998 |
2016 |
Cholestatic liver disease
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
58
|
|
0.040 |
None |
1.000 |
4 |
|
1996 |
2019 |
Cholestasis, Progressive Familial Intrahepatic, 2
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
4
|
25
|
0.040 |
None |
0.750 |
4 |
1
|
2009 |
2012 |