Cataract
|
disease |
Eye Diseases
|
Acquired Abnormality
|
878
|
124
|
0.020 |
None |
1.000 |
2 |
|
1999 |
2017 |
Cicatrix, Hypertrophic
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
185
|
3
|
0.020 |
None |
1.000 |
2 |
|
1996 |
2017 |
Nodule
|
phenotype |
|
Acquired Abnormality
|
278
|
19
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Disk, Herniated
|
disease |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
|
Acquired Abnormality
|
31
|
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Prolapsed lumbar disc
|
disease |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
|
Acquired Abnormality
|
75
|
33
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Superficial ulcer
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
242
|
10
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Muscle damage
|
phenotype |
|
Acquired Abnormality
|
163
|
4
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Mucosal erosion
|
phenotype |
|
Acquired Abnormality
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Hernia
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Anatomical Abnormality
|
136
|
10
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Hyperdistention
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Anatomical Abnormality
|
12
|
1
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
polyps
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Anatomical Abnormality
|
390
|
18
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Incontinentia Pigmenti Achromians
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
67
|
10
|
0.030 |
None |
1.000 |
3 |
|
2016 |
2017 |
Aniridia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
83
|
29
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Biliary Atresia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
|
Congenital Abnormality
|
184
|
32
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Atrial Septal Defects
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
384
|
96
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Microcephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Congenital Abnormality
|
1064
|
27
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Agenesis of corpus callosum
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Congenital Abnormality
|
615
|
45
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Congenital contractural arachnodactyly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
559
|
48
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Congenital posterior urethral valves
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Congenital Abnormality
|
26
|
1
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Aplasia Cutis Congenita
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
393
|
14
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Congenital laryngeal adductor palsy
|
disease |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Congenital Abnormality
|
17
|
|
0.010 |
None |
< 0.001 |
1 |
|
2013 |
2013 |
Congenital bilateral aplasia of vas deferens
|
disease |
Male Urogenital Diseases
|
Congenital Abnormality
|
27
|
210
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Congenital neurologic anomalies
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Congenital Abnormality
|
84
|
4
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Chiari malformation type II
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Congenital Abnormality
|
7
|
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Urban Schosser Spohn syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
6
|
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |