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: C0025467
Disease: Mesenteric Cyst
Mesenteric Cyst 		1 0 1 5.3E-02 0 0
CUI: C0036413
Disease: Scleredema Adultorum
Scleredema Adultorum 		1 0 1 5.3E-02 0 0
CUI: C0038557
Disease: Submandibular Gland Diseases
Submandibular Gland Diseases 		1 0 1 5.3E-02 0 0
CUI: C0206619
Disease: Lymphatic Vessel Tumors
Lymphatic Vessel Tumors 		1 0 1 5.3E-02 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 5.3E-02 0 0
CUI: C0232308
Disease: P pulmonale by EKG (finding)
P pulmonale by EKG (finding) 		1 0 1 5.3E-02 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 5.3E-02 0 0
CUI: C0265856
Disease: Hypoplasia of right heart
Hypoplasia of right heart 		1 0 1 5.3E-02 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus 		1 0 1 5.3E-02 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus 		1 0 1 5.3E-02 0 0
CUI: C0343263
Disease: Chondrolysis of articular cartilage
Chondrolysis of articular cartilage 		1 0 1 5.3E-02 0 0
CUI: C0523633
Disease: Fibronectin measurement
Fibronectin measurement 		1 0 1 5.3E-02 0 0
CUI: C0748427
Disease: Right atrial enlargement
Right atrial enlargement 		1 0 1 5.3E-02 0 0
CUI: C0795829
Disease: Chromosome 8, trisomy 8q
Chromosome 8, trisomy 8q 		1 0 1 5.3E-02 0 0
CUI: C0853856
Disease: Staphylococcal abscess
Staphylococcal abscess 		1 0 1 5.3E-02 0 0
CUI: C0869081
Disease: Congenital malformations of palate, not elsewhere classified in ICD10CM
Congenital malformations of palate, not elsewhere classified in ICD10CM 		1 0 1 5.3E-02 0 0
CUI: C0878515
Disease: Internal hydrocephalus
Internal hydrocephalus 		1 0 1 5.3E-02 0 0
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		1 0 1 5.3E-02 0 0
CUI: C1853508
Disease: ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2
ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2 		1 0 1 5.3E-02 0 0
CUI: C1853509
Disease: Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome
Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome 		1 0 1 5.3E-02 0 0
CUI: C1863495
Disease: Aplasia cutis congenita over posterior parietal area
Aplasia cutis congenita over posterior parietal area 		1 0 1 5.3E-02 0 0
CUI: C1863496
Disease: Aplasia cutis congenita on trunk or limbs
Aplasia cutis congenita on trunk or limbs 		1 0 1 5.3E-02 0 0
CUI: C1866075
Disease: GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder) 		1 0 1 5.3E-02 0 0
CUI: C1970625
Disease: Hypoplastic left atrium
Hypoplastic left atrium 		1 0 1 5.3E-02 0 0
CUI: C1970630
Disease: Agenesis of pulmonary vessels
Agenesis of pulmonary vessels 		1 0 1 5.3E-02 0 0