Talipes Calcaneovalgus
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Anatomical Abnormality
9
0.100
None
0
Hip Dysplasia
disease
Musculoskeletal Diseases; Wounds and Injuries
Anatomical Abnormality
128
16
0.100
None
0
Multiple congenital anomalies
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormality
251
350
0.100
None
1.000
5
2
2004
2015
Keratoderma
disease
Skin and Connective Tissue Diseases
Congenital Abnormality
24
2
0.020
None
1.000
2
1
2017
2018
Atrial Septal Defects
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
384
96
0.100
None
0
Ventricular Septal Defects
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
426
87
0.100
None
0
Microcephaly
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Congenital Abnormality
1064
27
0.100
None
0
Micrognathism
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
Congenital Abnormality
586
53
0.100
None
0
Low set ears
disease
Congenital Abnormality
489
64
0.100
None
0
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
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
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
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
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
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
Blood Coagulation Disorders
group
Hemic and Lymphatic Diseases
Disease or Syndrome
267
31
0.010
None
1.000
1
2015
2015
Cholestasis
disease
Digestive System Diseases
Disease or Syndrome
420
15
0.010
None
1.000
1
2019
2019
Intrahepatic Cholestasis
disease
Digestive System Diseases
Disease or Syndrome
54
3
0.010
None
1.000
1
2009
2009
Liver diseases
group
Digestive System Diseases
Disease or Syndrome
1019
100
0.010
None
1.000
1
2019
2019
Myocardial Infarction
disease
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Disease or Syndrome
1800
680
0.010
None
1.000
1
2018
2018
Tuberculosis
disease
Infections
Disease or Syndrome
1256
328
0.010
None
1.000
1
2008
2008
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
Intrahepatic biliary atresia
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
Disease or Syndrome
9
0.010
None
1.000
1
2005
2005
×
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