Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C3872848
Disease: Chronic pneumonitis of infancy
Chronic pneumonitis of infancy
1 0 1 1.00 0 0
CUI: C4024967
Disease: Congenital peripheral neuropathy
Congenital peripheral neuropathy
1 0 1 1.00 0 0
CUI: C1998122
Disease: Chronic respiratory insufficiency
Chronic respiratory insufficiency
2 0 1 0.50 0 0
CUI: C0555214
Disease: Multiple lung cysts
Multiple lung cysts
3 0 1 0.33 0 0
CUI: C0746105
Disease: Chronic interstitial lung disease
Chronic interstitial lung disease
3 0 1 0.33 0 0
Congenital Deficiency of Pulmonary Surfactant Protein B
3 0 1 0.33 0 0
Lipoid Proteinosis of Urbach and Wiethe
5 16 1 0.20 1 4.8E-02
Preterm Premature Rupture of Fetal Membranes
5 0 1 0.20 0 0
CUI: C2931829
Disease: RDS - infants
RDS - infants
6 0 1 0.17 0 0
Neuroendocrine cell hyperplasia of infancy
7 0 1 0.14 0 0
CUI: C0521648
Disease: Neonatal respiratory failure
Neonatal respiratory failure
8 0 1 0.12 0 0
CUI: C0238378
Disease: Desquamative interstitial pneumonia
Desquamative interstitial pneumonia
9 0 1 0.11 0 0
CUI: C3711368
Disease: Surfactant Dysfunction
Surfactant Dysfunction
10 0 1 1.0E-01 0 0
CUI: C0221227
Disease: Centriacinar Emphysema
Centriacinar Emphysema
14 0 1 7.1E-02 0 0
CUI: C0241984
Disease: Honeycomb lung
Honeycomb lung
14 0 1 7.1E-02 0 0
Ground-glass opacification on pulmonary HRCT
14 0 1 7.1E-02 0 0
CUI: C4476748
Disease: Reticular pattern on pulmonary HRCT
Reticular pattern on pulmonary HRCT
14 0 1 7.1E-02 0 0
CUI: C0020192
Disease: Hyaline Membrane Disease
Hyaline Membrane Disease
15 0 1 6.7E-02 0 0
CUI: C3806604
Disease: Infantile axial hypotonia
Infantile axial hypotonia
17 0 1 5.9E-02 0 0
CUI: C1301752
Disease: Respiratory morbidity
Respiratory morbidity
18 0 1 5.6E-02 0 0
CUI: C3274515
Disease: Severe Bronchopulmonary Dysplasia
Severe Bronchopulmonary Dysplasia
18 0 1 5.6E-02 0 0
CUI: C0394006
Disease: Dysequilibrium syndrome
Dysequilibrium syndrome
20 0 1 5.0E-02 0 0
CUI: C4721508
Disease: Hamman-Rich Disease
Hamman-Rich Disease
20 0 1 5.0E-02 0 0
CUI: C0034088
Disease: Pulmonary Valve Insufficiency
Pulmonary Valve Insufficiency
22 0 1 4.5E-02 0 0
Proximal muscle weakness in upper limbs
22 0 1 4.5E-02 0 0