Middle Cerebral Artery Occlusion
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
Acquired Abnormality
626
0.040
None
1.000
4
2017
2019
Cicatrix, Hypertrophic
disease
Pathological Conditions, Signs and Symptoms
Acquired Abnormality
185
3
0.030
None
1.000
3
1995
2006
Cataract
disease
Eye Diseases
Acquired Abnormality
878
124
0.020
None
1.000
2
2012
2018
Postoperative adhesion
phenotype
Pathological Conditions, Signs and Symptoms
Acquired Abnormality
9
0.010
None
1.000
1
2008
2008
Rheumatoid Nodule
disease
Skin and Connective Tissue Diseases; Musculoskeletal Diseases
Acquired Abnormality
26
3
0.010
None
1.000
1
2003
2003
×
CUI:
C0205204
Disease:
Scab
Scab
disease
Acquired Abnormality
24
0.010
None
1.000
1
2018
2018
Prolapsed lumbar disc
disease
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
Acquired Abnormality
75
33
0.010
None
1.000
1
2017
2017
Anastomosis
disease
Acquired Abnormality
155
2
0.010
None
1.000
1
2019
2019
Air cyst
disease
Pathological Conditions, Signs and Symptoms; Neoplasms
Acquired Abnormality
4
1
0.010
None
1.000
1
2009
2009
Superficial ulcer
disease
Pathological Conditions, Signs and Symptoms
Acquired Abnormality
242
10
0.010
None
1.000
1
1
2020
2020
Epiretinal Membrane
disease
Eye Diseases
Acquired Abnormality
102
0.010
None
1.000
1
2017
2017
Hyperplastic lymph node
disease
Acquired Abnormality
12
0.010
None
1.000
1
1993
1993
Skin callus
disease
Skin and Connective Tissue Diseases
Acquired Abnormality
154
0.010
None
1.000
1
2018
2018
Carotid Artery Plaque
disease
Nervous System Diseases; Cardiovascular Diseases
Acquired Abnormality
41
3
0.010
None
1.000
1
2014
2014
Hernia
phenotype
Pathological Conditions, Signs and Symptoms
Anatomical Abnormality
136
10
0.010
None
1.000
1
1
2017
2017
Other ureteric obstruction
phenotype
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Anatomical Abnormality
52
0.200
None
1.000
1
2011
2011
polyps
phenotype
Pathological Conditions, Signs and Symptoms
Anatomical Abnormality
390
18
0.010
None
1.000
1
2018
2018
Subglottic stenosis
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
Anatomical Abnormality
17
2
0.010
None
1.000
1
2017
2017
Biliary stricture
disease
Digestive System Diseases
Anatomical Abnormality
17
0.010
None
1.000
1
2012
2012
Fibromatosis, Gingival
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
Anatomical Abnormality
20
1
0.100
None
0
Nerve Degeneration
phenotype
Pathological Conditions, Signs and Symptoms
Cell or Molecular Dysfunction
165
17
0.300
None
1.000
3
2004
2009
Biliary Atresia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
Congenital Abnormality
184
32
0.060
None
0.833
6
2002
2018
Congenital atresia of extrahepatic bile duct
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
Congenital Abnormality
172
19
0.060
None
0.833
6
2002
2018
MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Nervous System Diseases
Congenital Abnormality
24
46
0.030
None
1.000
3
2014
2019
FRONTOMETAPHYSEAL DYSPLASIA 1
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Congenital Abnormality
28
3
0.030
None
1.000
3
2018
2018