Systemic Scleroderma
disease
Skin and Connective Tissue Diseases
Disease or Syndrome
979
287
0.010
None
1.000
1
1
2016
2016
Chronic Obstructive Airway Disease
disease
Respiratory Tract Diseases
Disease or Syndrome
1428
852
0.100
None
1.000
2
2
2019
2019
Lung Diseases, Interstitial
group
Respiratory Tract Diseases
Disease or Syndrome
319
144
0.100
None
1.000
1
3
2013
2013
Idiopathic Pulmonary Fibrosis
disease
Respiratory Tract Diseases
Disease or Syndrome
803
63
0.500
None
1.000
1
2013
2013
Hamman-Rich Disease
disease
Respiratory Tract Diseases
Disease or Syndrome
20
0.300
None
1.000
1
2013
2013
Usual Interstitial Pneumonia
disease
Respiratory Tract Diseases
Disease or Syndrome
64
2
0.300
None
1.000
1
2013
2013
Familial Idiopathic Pulmonary Fibrosis
disease
Respiratory Tract Diseases
Disease or Syndrome
23
0.300
None
1.000
1
2013
2013
Bronchiectasis
disease
Respiratory Tract Diseases
Disease or Syndrome
190
15
0.100
None
0
Pulmonary Fibrosis
disease
Respiratory Tract Diseases
Disease or Syndrome
924
25
0.100
None
0
Honeycomb lung
disease
Respiratory Tract Diseases
Disease or Syndrome
14
0.100
None
0
Coughing
phenotype
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
Sign or Symptom
235
16
0.100
None
0
Dyspnea on exertion
phenotype
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
Sign or Symptom
102
3
0.100
None
0
Hyperactive behavior
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Mental or Behavioral Dysfunction
1263
112
0.010
None
1.000
1
2003
2003
Ataxia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
868
68
0.100
None
0
Dystonia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
453
97
0.100
None
0
Leukemogenesis
disease
Pathological Conditions, Signs and Symptoms; Neoplasms
Neoplastic Process
996
25
0.010
None
1.000
1
2016
2016
Muscle Spasticity
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Sign or Symptom
580
48
0.100
None
0
Hamman-Rich syndrome
disease
Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases
Disease or Syndrome
55
8
0.300
None
1.000
1
2013
2013
Gastrointestinal Hemorrhage
phenotype
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Pathologic Function
122
24
0.100
None
0
CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS (disorder)
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
6
3
0.510
None
1.000
2
2015
2016
Fetal Growth Retardation
phenotype
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Disease or Syndrome
1037
21
0.100
None
0
×
CUI:
C0034642
Disease:
Rales
Rales
phenotype
Pathological Conditions, Signs and Symptoms
Finding
23
0.100
None
0
Osteopenia
disease
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
845
61
0.100
None
0
Diabetes Mellitus, Non-Insulin-Dependent
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Disease or Syndrome
3134
2672
0.010
None
1.000
1
2013
2013
Cerebral Palsy
disease
Nervous System Diseases
Disease or Syndrome
241
69
0.010
None
1.000
1
2
2019
2019