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: C1321313
Disease: Astrocytic hamartoma
Astrocytic hamartoma 		1 0 1 0.50 0 0
CUI: C1861316
Disease: Radially deviated wrists
Radially deviated wrists 		1 0 1 0.50 0 0
CUI: C0740441
Disease: Acute diarrhea
Acute diarrhea 		4 0 1 0.20 0 0
CUI: C1865702
Disease: Joint contracture of the 5th finger
Joint contracture of the 5th finger 		4 0 1 0.20 0 0
CUI: C4021742
Disease: Abnormality of the humerus
Abnormality of the humerus 		10 0 2 0.20 0 0
CUI: C1840535
Disease: Abnormality of the carpal bones
Abnormality of the carpal bones 		6 0 1 0.14 0 0
CUI: C4025662
Disease: Abnormality of the ulna
Abnormality of the ulna 		14 0 2 0.14 0 0
CUI: C0265633
Disease: Congenital absence of tibia
Congenital absence of tibia 		7 0 1 0.12 0 0
CUI: C0432055
Disease: Simple syndactyly of fingers - first web
Simple syndactyly of fingers - first web 		9 0 1 1.0E-01 0 0
CUI: C1836193
Disease: Synostosis of carpal bones
Synostosis of carpal bones 		23 0 2 8.7E-02 0 0
CUI: C0264122
Disease: Atrophy, Disuse
Atrophy, Disuse 		16 0 1 5.9E-02 0 0
CUI: C3489630
Disease: Somatotrophinoma, Familial
Somatotrophinoma, Familial 		18 0 1 5.3E-02 0 0
CUI: C1846534
Disease: ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1 		20 0 1 4.8E-02 0 0
CUI: C2749463
Disease: Aplasia/Hypoplasia of the radius
Aplasia/Hypoplasia of the radius 		45 0 2 4.4E-02 0 0
CUI: C0267187
Disease: Intestinal metaplasia of gastric mucosa
Intestinal metaplasia of gastric mucosa 		35 0 1 2.8E-02 0 0
CUI: C1851100
Disease: LAURIN-SANDROW SYNDROME
LAURIN-SANDROW SYNDROME 		36 0 1 2.7E-02 0 0
CUI: C0265797
Disease: Congenital emphysema
Congenital emphysema 		40 0 1 2.4E-02 0 0
CUI: C0242387
Disease: Mandibulofacial Dysostosis
Mandibulofacial Dysostosis 		42 0 1 2.3E-02 0 0
CUI: C1456246
Disease: Bacteroides fragilis infection in conditions classified elsewhere and of unspecified site
Bacteroides fragilis infection in conditions classified elsewhere and of unspecified site 		43 0 1 2.3E-02 0 0
CUI: C1849039
Disease: Metaphyseal widening
Metaphyseal widening 		43 0 1 2.3E-02 0 0
CUI: C0023794
Disease: Lipoidosis
Lipoidosis 		44 0 1 2.2E-02 0 0
CUI: C0345354
Disease: Radial polydactyly
Radial polydactyly 		51 0 1 1.9E-02 0 0
CUI: C0206762
Disease: Limb Deformities, Congenital
Limb Deformities, Congenital 		59 0 1 1.7E-02 0 0
CUI: C1858991
Disease: Childhood Ataxia with Central Nervous System Hypomyelinization
Childhood Ataxia with Central Nervous System Hypomyelinization 		59 0 1 1.7E-02 0 0
CUI: C0409952
Disease: Idiopathic osteoarthritis
Idiopathic osteoarthritis 		63 0 1 1.6E-02 0 0