Bronchitis in children
|
disease |
|
Disease or Syndrome
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Xeroderma
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
7
|
1
|
0.020 |
None |
1.000 |
2 |
1
|
2005 |
2007 |
Malignant neoplasm of upper lobe, bronchus or lung
|
disease |
Neoplasms; Respiratory Tract Diseases
|
Neoplastic Process
|
7
|
|
0.200 |
None |
1.000 |
1 |
|
2005 |
2005 |
Malignant neoplasm of middle lobe, bronchus or lung
|
disease |
Neoplasms; Respiratory Tract Diseases
|
Neoplastic Process
|
7
|
|
0.200 |
None |
1.000 |
1 |
|
2005 |
2005 |
Malignant neoplasm of lower lobe, bronchus or lung
|
disease |
Neoplasms; Respiratory Tract Diseases
|
Neoplastic Process
|
7
|
|
0.200 |
None |
1.000 |
1 |
|
2005 |
2005 |
Malignant neoplasm of other parts of bronchus or lung
|
disease |
Neoplasms; Respiratory Tract Diseases
|
Neoplastic Process
|
7
|
|
0.200 |
None |
1.000 |
1 |
|
2005 |
2005 |
Xeroderma pigmentosum, group F
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
8
|
31
|
0.010 |
None |
1.000 |
1 |
2
|
2019 |
2019 |
Flat nasal alae
|
phenotype |
|
Finding
|
8
|
|
0.100 |
None |
|
0 |
|
|
|
Defective DNA repair after ultraviolet radiation damage
|
phenotype |
|
Finding
|
12
|
|
0.100 |
None |
|
0 |
|
|
|
Amino Acid Metabolism, Inherited Disorders
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
13
|
|
0.300 |
None |
1.000 |
1 |
|
1998 |
1998 |
Autosome Abnormalities
|
group |
Pathological Conditions, Signs and Symptoms
|
Cell or Molecular Dysfunction
|
16
|
|
0.300 |
None |
1.000 |
1 |
|
2010 |
2010 |
Chromosome Aberrations
|
group |
Pathological Conditions, Signs and Symptoms
|
Cell or Molecular Dysfunction
|
16
|
|
0.300 |
None |
1.000 |
1 |
|
2010 |
2010 |
Entropion
|
disease |
Eye Diseases
|
Disease or Syndrome
|
18
|
1
|
0.100 |
None |
|
0 |
|
|
|
Congenital ankyloblepharon
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
18
|
|
0.100 |
None |
|
0 |
|
|
|
Ankyloblepharon
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Anatomical Abnormality
|
18
|
|
0.100 |
None |
|
0 |
|
|
|
Amino Acid Metabolism, Inborn Errors
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
20
|
|
0.300 |
None |
1.000 |
1 |
|
1998 |
1998 |
Conjunctival telangiectasis
|
disease |
|
Disease or Syndrome
|
20
|
1
|
0.100 |
None |
|
0 |
|
|
|
Poikiloderma
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
20
|
2
|
0.100 |
None |
|
0 |
|
|
|
Poikiloderma of Kindler
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Stomatognathic Diseases
|
Disease or Syndrome
|
21
|
25
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Eye Neoplasms
|
group |
Neoplasms; Eye Diseases
|
Neoplastic Process
|
24
|
|
0.100 |
None |
|
0 |
|
|
|
Craniofacial hyperostosis
|
phenotype |
|
Finding
|
25
|
|
0.100 |
None |
|
0 |
|
|
|
Micronuclei, Chromosome-Defective
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Cell Component
|
26
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Micronuclei, Genotoxicant-Induced
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Cell Component
|
26
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Trichothiodystrophy Syndromes
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
33
|
15
|
0.030 |
None |
1.000 |
3 |
|
2003 |
2008 |
Coronavirus Infections
|
group |
Infections
|
Disease or Syndrome
|
33
|
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |