Urethral obstruction sequence
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Aplasia of the abdominal wall musculature
|
phenotype |
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Congenital anomaly of the bladder
|
group |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Congenital Abnormality
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Cervical auricle (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
INJECTED EYE
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases
|
Sign or Symptom
|
6
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Abdominal Cryptorchidism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
8
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Inguinal Cryptorchidism
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases
|
Finding
|
8
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Megacystis microcolon intestinal hypoperistalsis syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
|
Disease or Syndrome
|
9
|
3
|
0.200 |
None |
1.000 |
1 |
|
2000 |
2000 |
Acquired hallux valgus
|
disease |
Musculoskeletal Diseases
|
Acquired Abnormality
|
14
|
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Congenital hallux valgus
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
14
|
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Neuro-Behcet disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
15
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Mucopolysaccharidosis III
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
17
|
15
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Unilateral Cryptorchidism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
17
|
5
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Soluble Interleukin 6 Receptor Measurement
|
phenotype |
|
Laboratory Procedure
|
17
|
25
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
brain cyst
|
disease |
|
Disease or Syndrome
|
18
|
|
0.060 |
None |
1.000 |
6 |
|
2011 |
2019 |
Urogenital sinus anomaly
|
disease |
|
Anatomical Abnormality
|
18
|
|
0.100 |
None |
|
0 |
|
|
|
Intestinal Atresia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
|
Disease or Syndrome
|
20
|
2
|
0.100 |
None |
|
0 |
|
|
|
Dental White Spot
|
disease |
Stomatognathic Diseases
|
Disease or Syndrome
|
22
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Nonarteritic anterior ischemic optic neuropathy (NAION)
|
disease |
|
Disease or Syndrome
|
22
|
6
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Urinary Bladder Diseases
|
group |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
24
|
|
0.320 |
None |
1.000 |
2 |
|
2011 |
2019 |
Mydriasis
|
phenotype |
Eye Diseases
|
Sign or Symptom
|
25
|
2
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
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
|
0.100 |
None |
|
0 |
|
|
|
Acute pneumonia
|
disease |
Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
29
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Aplasia/Hypoplasia of the lungs
|
phenotype |
|
Finding
|
29
|
|
0.100 |
None |
|
0 |
|
|
|
Postoperative Nausea and Vomiting
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
31
|
18
|
0.020 |
None |
1.000 |
2 |
1
|
2014 |
2018 |