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: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 2 6.1E-02 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 2 6.1E-02 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 2 6.1E-02 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 4 5.9E-02 0 0
CUI: C0175707
Disease: Asplenia Syndrome
Asplenia Syndrome 		13 0 1 5.9E-02 0 0
CUI: C0852413
Disease: Abnormal muscle tone
Abnormal muscle tone 		14 0 1 5.6E-02 0 0
CUI: C4317124
Disease: Polynesian Bronchiectasis
Polynesian Bronchiectasis 		35 0 2 5.3E-02 0 0
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen 		80 0 4 4.9E-02 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 4 4.8E-02 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 8 5 4.8E-02 2 0.25
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		39 0 2 4.8E-02 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 2 4.8E-02 0 0
CUI: C4520981
Disease: Abnormality of the basal ganglia
Abnormality of the basal ganglia 		17 0 1 4.8E-02 0 0
CUI: C0009080
Disease: Clubbed Fingers
Clubbed Fingers 		88 0 4 4.5E-02 0 0
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		43 0 2 4.3E-02 0 0
CUI: C0600260
Disease: Lung Diseases, Obstructive
Lung Diseases, Obstructive 		104 0 4 3.8E-02 0 0
CUI: C0029883
Disease: Otitis Media with Effusion
Otitis Media with Effusion 		110 0 4 3.6E-02 0 0
CUI: C0010036
Disease: Corneal dystrophy
Corneal dystrophy 		113 0 4 3.5E-02 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		55 0 2 3.4E-02 0 0
CUI: C0008677
Disease: Bronchitis, Chronic
Bronchitis, Chronic 		118 0 4 3.4E-02 0 0
CUI: C0009451
Disease: Communicating Hydrocephalus
Communicating Hydrocephalus 		26 0 1 3.3E-02 0 0
CUI: C0280451
Disease: de novo myelodysplastic syndromes
de novo myelodysplastic syndromes 		27 0 1 3.2E-02 0 0
CUI: C4551720
Disease: Primary Ciliary Dyskinesia
Primary Ciliary Dyskinesia 		160 0 5 3.1E-02 0 0
CUI: C0271441
Disease: Chronic otitis media
Chronic otitis media 		163 6 5 3.1E-02 1 0.14
CUI: C0021359
Disease: Infertility
Infertility 		130 0 4 3.1E-02 0 0