Adult Liver Carcinoma
disease
Digestive System Diseases; Neoplasms
Neoplastic Process
1377
72
0.010
None
1.000
1
2018
2018
AIDS related complex
disease
Infections; Immune System Diseases
Disease or Syndrome
100
43
0.100
None
1.000
10
2004
2019
Arthrogryposis
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Disease or Syndrome
198
33
0.460
strong
1.000
7
2004
2019
Arthrogryposis with renal dysfunction and cholestasis syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Disease or Syndrome
12
0.100
None
1.000
16
2004
2019
Arthrogryposis, renal dysfunction, and cholestasis 1
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases
Disease or Syndrome
16
13
1.000
None
1.000
26
13
2004
2019
Atrial Septal Defects
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
384
96
0.100
None
0
Blood Coagulation Disorders
group
Hemic and Lymphatic Diseases
Disease or Syndrome
267
31
0.010
None
1.000
1
2015
2015
×
CUI:
C1968949
Disease:
Cakut
Cakut
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
72
8
0.300
strong
1.000
1
2009
2009
Cholestasis
disease
Digestive System Diseases
Disease or Syndrome
420
15
0.010
None
1.000
1
2019
2019
Cholestatic liver disease
disease
Digestive System Diseases
Disease or Syndrome
58
0.100
None
0
Chronic Kidney Diseases
group
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
1074
306
0.010
None
1.000
1
2018
2018
Colorectal Carcinoma
disease
Digestive System Diseases; Neoplasms
Neoplastic Process
5473
1962
0.010
None
1.000
1
2020
2020
Congenital ichthyosis
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Disease or Syndrome
80
11
0.040
None
1.000
4
1
2006
2018
Conjugated hyperbilirubinemia
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
32
1
0.100
None
0
Death in infancy
phenotype
Finding
146
7
0.100
None
0
Dehydration
phenotype
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
Disease or Syndrome
295
6
0.100
None
0
Diabetes Mellitus, Non-Insulin-Dependent
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Disease or Syndrome
3134
2672
0.100
None
1.000
2
1
2012
2014
Elevated hepatic transaminase
phenotype
Finding
212
9
0.100
None
0
Failure to Thrive
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
842
10
0.100
None
0
Generalized hypotonia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
955
164
0.100
None
0
Global developmental delay
disease
Mental or Behavioral Dysfunction
1825
553
0.100
None
0
Hepatocarcinogenesis
disease
Pathological Conditions, Signs and Symptoms; Neoplasms
Neoplastic Process
855
24
0.010
None
1.000
1
2018
2018
Hip Dysplasia
disease
Musculoskeletal Diseases; Wounds and Injuries
Anatomical Abnormality
128
16
0.100
None
0
Ichthyoses
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Disease or Syndrome
194
18
0.140
None
1.000
4
1
2006
2018
Icterus
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
241
17
0.100
None
0