Arterial calcification of infancy
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
3
2
0.580
None
1.000
9
2011
2020
Gronblad-Strandberg Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
Disease or Syndrome
3
0.300
None
1.000
8
2002
2015
Metabolic Diseases
group
Nutritional and Metabolic Diseases
Disease or Syndrome
945
50
0.050
None
0.800
5
2001
2017
Leukemia, Myelocytic, Acute
disease
Neoplasms
Neoplastic Process
3111
6892
0.050
None
0.800
5
2000
2020
Rheumatoid Arthritis
disease
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
Disease or Syndrome
2723
2387
0.030
None
1.000
3
1988
2017
leukemia
disease
Neoplasms
Neoplastic Process
2111
144
0.020
None
1.000
2
1996
2020
Osteoporosis
disease
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
1098
182
0.010
None
1.000
1
2015
2015
×
CUI:
C0030193
Disease:
Pain
Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1554
196
0.010
None
1.000
1
2017
2017
Obesity
disease
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
Disease or Syndrome
2821
1111
0.010
None
1.000
1
2018
2018
Neutropenia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
389
97
0.010
None
1.000
1
2017
2017
Neoplasms
group
Neoplasms
Neoplastic Process
10161
1644
0.010
None
1.000
1
2007
2007
Lymphadenopathy
phenotype
Hemic and Lymphatic Diseases
Disease or Syndrome
277
5
0.010
None
1.000
1
2003
2003
Peripheral Arterial Diseases
group
Cardiovascular Diseases
Disease or Syndrome
319
128
0.010
None
1.000
1
2019
2019
Hepatitis B, Chronic
disease
Digestive System Diseases; Infections
Disease or Syndrome
415
84
0.010
None
1.000
1
1986
1986
Keratoconjunctivitis
disease
Eye Diseases
Disease or Syndrome
16
3
0.010
None
1.000
1
2017
2017
Meningomyelocele
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
89
27
0.010
None
1.000
1
1998
1998
Lupus Erythematosus, Systemic
disease
Skin and Connective Tissue Diseases; Immune System Diseases
Disease or Syndrome
1883
1172
0.010
None
1.000
1
1987
1987
Lupus Erythematosus, Discoid
disease
Skin and Connective Tissue Diseases
Disease or Syndrome
552
46
0.010
None
1.000
1
1987
1987
Liver diseases
group
Digestive System Diseases
Disease or Syndrome
1019
100
0.010
None
< 0.001
1
2018
2018
Leukopenia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
440
153
0.010
None
1.000
1
2017
2017
Myeloid Leukemia, Chronic
disease
Neoplasms; Hemic and Lymphatic Diseases
Neoplastic Process
1172
115
0.010
None
1.000
1
1995
1995
Pelvic Neoplasms
group
Neoplasms
Neoplastic Process
12
0.010
None
1.000
1
2018
2018
Familial Mediterranean Fever
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Disease or Syndrome
133
82
0.010
None
1.000
1
2007
2007
Vascular calcification
phenotype
Nutritional and Metabolic Diseases
Disease or Syndrome
257
3
0.010
None
1.000
1
2017
2017
Polycystic Kidney, Autosomal Dominant
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
280
35
0.010
None
1.000
1
2008
2008