Source: ALL
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: C4552030
Disease: Ciliary Dyskinesia, Primary, 7, With Or Without Situs Inversus
Ciliary Dyskinesia, Primary, 7, With Or Without Situs Inversus 		1 0 1 0.50 0 0
CUI: C4693994
Disease: CILIARY DYSKINESIA, PRIMARY, 7, WITH SITUS INVERSUS
CILIARY DYSKINESIA, PRIMARY, 7, WITH SITUS INVERSUS 		1 0 1 0.50 0 0
CUI: C4025885
Disease: Abnormality of the uvula
Abnormality of the uvula 		2 2 1 0.33 2 0.14
CUI: C0149514
Disease: Acute bronchitis
Acute bronchitis 		4 2 1 0.20 2 0.14
CUI: C0578475
Disease: Cyanotic attack
Cyanotic attack 		4 3 1 0.20 2 0.13
CUI: C3812686
Disease: Interleukin 1 Receptor Antagonist Measurement
Interleukin 1 Receptor Antagonist Measurement 		6 0 1 0.14 0 0
CUI: C0004099
Disease: Asthma, Exercise-Induced
Asthma, Exercise-Induced 		8 3 1 0.11 2 0.13
CUI: C4022983
Disease: Abnormal ciliary motility
Abnormal ciliary motility 		9 5 1 1.0E-01 2 0.12
CUI: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx 		13 0 1 7.1E-02 0 0
CUI: C0478019
Disease: Other specified congenital malformations of respiratory system
Other specified congenital malformations of respiratory system 		13 0 1 7.1E-02 0 0
CUI: C0030489
Disease: Paraproteinemias
Paraproteinemias 		14 0 1 6.7E-02 0 0
CUI: C0235063
Disease: Respiratory Depression
Respiratory Depression 		24 5 1 4.0E-02 2 0.12
CUI: C0598784
Disease: Dyslipoproteinemias
Dyslipoproteinemias 		24 0 1 4.0E-02 0 0
CUI: C4025860
Disease: Hearing abnormality
Hearing abnormality 		24 5 1 4.0E-02 2 0.12
CUI: C4054546
Disease: Melanocortin 4 Receptor Deficiency
Melanocortin 4 Receptor Deficiency 		24 28 1 4.0E-02 2 5.0E-02
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 402 2 3.4E-02 8 2.0E-02
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 1 3.3E-02 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 1 3.3E-02 0 0
CUI: C0149781
Disease: Spontaneous pneumothorax
Spontaneous pneumothorax 		30 6 1 3.2E-02 2 0.11
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 1 3.2E-02 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 1 3.2E-02 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 1 3.2E-02 0 0
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly 		35 0 1 2.8E-02 0 0
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		39 0 1 2.5E-02 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 2.5E-02 0 0