VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF
|
phenotype |
|
Finding
|
1
|
4
|
0.100 |
None |
1.000 |
38 |
4
|
1995 |
2017 |
Atypical cystic fibrosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases
|
Disease or Syndrome
|
1
|
5
|
0.050 |
None |
1.000 |
5 |
5
|
2001 |
2013 |
Young Syndrome
|
disease |
Infections; Male Urogenital Diseases; Respiratory Tract Diseases
|
Disease or Syndrome
|
1
|
|
0.020 |
None |
0.500 |
2 |
|
1996 |
1998 |
congenital obstruction
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Distal intestinal obstruction syndrome
|
disease |
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Acquired obstructive azoospermia
|
disease |
Male Urogenital Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Hypotonic dehydration
|
disease |
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
1995 |
1995 |
Gastrointestinal cramps
|
phenotype |
|
Sign or Symptom
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Bronchopulmonary infection
|
disease |
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2003 |
2003 |
Classical cystic fibrosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases
|
Disease or Syndrome
|
1
|
3
|
0.010 |
None |
1.000 |
1 |
3
|
2010 |
2010 |
Left renal agenesis
|
disease |
|
Congenital Abnormality
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Pulmonary embolism with pulmonary infarction
|
phenotype |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Acute bronchitis and bronchiolitis
|
disease |
|
Disease or Syndrome
|
1
|
2
|
0.100 |
None |
|
0 |
2
|
|
|
Anal and rectal conditions
|
disease |
|
Disease or Syndrome
|
1
|
2
|
0.100 |
None |
|
0 |
2
|
|
|
HYPERTRYPSINEMIA, NEONATAL, SUSCEPTIBILITY TO
|
phenotype |
|
Finding
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
SWEAT CHLORIDE ELEVATION WITHOUT CYSTIC FIBROSIS
|
disease |
|
Finding
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
PANCREATITIS, IDIOPATHIC, SUSCEPTIBILITY TO
|
phenotype |
|
Finding
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1, MODIFIER OF
|
phenotype |
|
Finding
|
1
|
2
|
0.100 |
None |
|
0 |
2
|
|
|
bilateral agenesis
|
disease |
|
Congenital Abnormality
|
2
|
|
0.020 |
None |
1.000 |
2 |
|
2006 |
2011 |
Infectious disorder of bronchus
|
group |
Respiratory Tract Diseases
|
Disease or Syndrome
|
2
|
|
0.020 |
None |
1.000 |
2 |
|
2004 |
2006 |
Hypochloremic alkalosis
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
2
|
1
|
0.010 |
None |
1.000 |
1 |
1
|
2018 |
2018 |
Chronic pulmonary heart disease
|
disease |
Respiratory Tract Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
1
|
0.010 |
None |
1.000 |
1 |
1
|
2014 |
2014 |
Deficiency of prolidase
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Disease or Syndrome
|
2
|
12
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Congenital unilateral absence
|
disease |
|
Congenital Abnormality
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Pseudo-Bartter syndrome
|
disease |
|
Disease or Syndrome
|
2
|
2
|
0.010 |
None |
1.000 |
1 |
2
|
2019 |
2019 |