Abnormality of the dentition
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
Finding
140
16
0.100
None
0
Abnormality of the voice
disease
Finding
64
0.100
None
0
Absence Seizures
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
205
8
0.300
None
1.000
2
1995
2016
Adult hypophosphatasia (disorder)
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Disease or Syndrome
9
57
0.950
None
0.975
40
56
1988
2019
Adult Rickets
disease
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
47
0.100
None
0
Agenesis
disease
Congenital Abnormality
161
44
0.010
None
1.000
1
2007
2007
Alkaline phosphatase measurement
phenotype
Laboratory Procedure
42
79
0.100
None
1.000
3
3
2010
2019
Alveolar Bone Loss
disease
Musculoskeletal Diseases; Stomatognathic Diseases
Disease or Syndrome
101
0.300
None
1.000
1
2010
2010
Anemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
847
94
0.100
None
0
Ankylosing spondylitis
disease
Musculoskeletal Diseases
Disease or Syndrome
710
609
0.050
None
0.800
5
3
2007
2018
Anorexia
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
242
10
0.100
None
0
Anxiety
disease
Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
1048
287
0.010
None
1.000
1
2015
2015
Anxiety Disorders
group
Mental Disorders
Mental or Behavioral Dysfunction
840
163
0.010
None
1.000
1
2015
2015
×
CUI:
C0003578
Disease:
Apnea
Apnea
phenotype
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
Sign or Symptom
262
11
0.110
None
1.000
1
2011
2011
Arteriosclerosis
disease
Cardiovascular Diseases
Disease or Syndrome
2006
267
0.010
None
1.000
1
2019
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
0.010
None
1.000
1
2019
2019
Arthropathy
group
Musculoskeletal Diseases
Disease or Syndrome
187
10
0.100
None
0
Asthma
disease
Respiratory Tract Diseases; Immune System Diseases
Disease or Syndrome
2096
1536
0.020
None
1.000
2
2014
2019
Asthmatic pulmonary eosinophilia
disease
Respiratory Tract Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
62
1
0.010
None
1.000
1
2014
2014
Atherosclerosis
disease
Cardiovascular Diseases
Disease or Syndrome
2044
281
0.010
None
1.000
1
2019
2019
Atonic Absence Seizures
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
102
0.300
None
1.000
2
1995
2016
Blue sclera
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Finding
70
13
0.100
None
0
Bone Diseases
group
Musculoskeletal Diseases
Disease or Syndrome
317
10
0.050
None
1.000
5
1
2000
2019
Breast Carcinoma
disease
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
6776
2793
0.010
None
1.000
1
1993
1993
Calcinosis
phenotype
Nutritional and Metabolic Diseases
Pathologic Function
52
0.300
None
1.000
1
2011
2011