Ciliary Dyskinesia, Primary, 7, With Or Without Situs Inversus
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
|
0.700 |
None |
1.000 |
1 |
|
1999 |
1999 |
CILIARY DYSKINESIA, PRIMARY, 7, WITH SITUS INVERSUS
|
disease |
|
Disease or Syndrome
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
CILIARY DYSKINESIA, PRIMARY, 7 (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
14
|
0.900 |
None |
1.000 |
5 |
14
|
1999 |
2014 |
Abnormality of the uvula
|
phenotype |
|
Anatomical Abnormality
|
2
|
2
|
0.100 |
None |
|
0 |
2
|
|
|
Acute bronchitis
|
disease |
Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
4
|
2
|
0.100 |
None |
|
0 |
2
|
|
|
Cyanotic attack
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
4
|
3
|
0.100 |
None |
|
0 |
2
|
|
|
Interleukin 1 Receptor Antagonist Measurement
|
phenotype |
|
Laboratory Procedure
|
6
|
11
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
Asthma, Exercise-Induced
|
disease |
Respiratory Tract Diseases; Immune System Diseases
|
Disease or Syndrome
|
8
|
3
|
0.100 |
None |
|
0 |
2
|
|
|
Abnormal ciliary motility
|
disease |
|
Anatomical Abnormality
|
9
|
5
|
0.100 |
None |
|
0 |
2
|
|
|
Congenital atresia of nasopharynx
|
disease |
Stomatognathic Diseases; Otorhinolaryngologic Diseases
|
Congenital Abnormality
|
13
|
|
0.200 |
None |
1.000 |
1 |
|
1999 |
1999 |
Other specified congenital malformations of respiratory system
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
|
Congenital Abnormality
|
13
|
|
0.200 |
None |
1.000 |
1 |
|
1999 |
1999 |
Paraproteinemias
|
disease |
Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
14
|
9
|
0.100 |
None |
1.000 |
1 |
1
|
2015 |
2015 |
Dyslipoproteinemias
|
phenotype |
Nutritional and Metabolic Diseases
|
Pathologic Function
|
24
|
|
0.300 |
None |
1.000 |
1 |
|
2009 |
2009 |
Respiratory Depression
|
phenotype |
Respiratory Tract Diseases
|
Pathologic Function
|
24
|
5
|
0.100 |
None |
|
0 |
2
|
|
|
Hearing abnormality
|
disease |
|
Finding
|
24
|
5
|
0.100 |
None |
|
0 |
2
|
|
|
Melanocortin 4 Receptor Deficiency
|
phenotype |
|
Finding
|
24
|
28
|
0.100 |
None |
|
0 |
2
|
|
|
Heterotaxy, Visceral, 3, Autosomal
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
29
|
|
0.200 |
None |
|
0 |
|
|
|
HETEROTAXY, VISCERAL, 4, AUTOSOMAL
|
disease |
|
Disease or Syndrome
|
29
|
2
|
0.200 |
None |
|
0 |
|
|
|
Spontaneous pneumothorax
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
30
|
6
|
0.100 |
None |
|
0 |
2
|
|
|
HETEROTAXY, VISCERAL, 1, X-LINKED
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
30
|
17
|
0.200 |
None |
|
0 |
|
|
|
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
|
disease |
|
Disease or Syndrome
|
30
|
3
|
0.200 |
None |
|
0 |
|
|
|
HETEROTAXY, VISCERAL, 6, AUTOSOMAL
|
disease |
|
Disease or Syndrome
|
30
|
2
|
0.200 |
None |
|
0 |
|
|
|
Heterotaxy Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
39
|
8
|
0.210 |
None |
1.000 |
1 |
|
2019 |
2019 |
HETEROTAXY, VISCERAL, 2, AUTOSOMAL
|
disease |
|
Disease or Syndrome
|
39
|
5
|
0.200 |
None |
|
0 |
|
|
|
Recurrent sinusitis
|
disease |
Infections; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
41
|
3
|
0.100 |
None |
|
0 |
2
|
|
|