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: C0242490
Disease: Enthesopathy
Enthesopathy 		0 1 0 0 1 5.0E-02
CUI: C0268958
Disease: Acute orchitis
Acute orchitis 		0 1 0 0 1 5.0E-02
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania 		0 1 0 0 1 5.0E-02
CUI: C0877781
Disease: Hemicrania
Hemicrania 		0 1 0 0 1 5.0E-02
CUI: C2585575
Disease: Recurrent abdominal pain
Recurrent abdominal pain 		0 2 0 0 1 4.8E-02
CUI: C0040947
Disease: Trichostrongyloidiasis
Trichostrongyloidiasis 		1 0 1 1.7E-02 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 1 1 1.7E-02 1 5.0E-02
CUI: C0233283
Disease: Complete breech presentation
Complete breech presentation 		1 1 1 1.7E-02 1 5.0E-02
CUI: C0234516
Disease: Speech dysfunction
Speech dysfunction 		1 0 1 1.7E-02 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 1.7E-02 0 0
CUI: C0268090
Disease: Manganese deficiency
Manganese deficiency 		1 0 1 1.7E-02 0 0
CUI: C0275703
Disease: Brazilian purpuric fever
Brazilian purpuric fever 		1 0 1 1.7E-02 0 0
CUI: C0341266
Disease: Diverticulosis of the duodenum
Diverticulosis of the duodenum 		1 1 1 1.7E-02 1 5.0E-02
CUI: C0393693
Disease: Benign Neonatal Epilepsy, Nonfamilial
Benign Neonatal Epilepsy, Nonfamilial 		1 0 1 1.7E-02 0 0
CUI: C0730309
Disease: Inherited optic neuropathy
Inherited optic neuropathy 		1 0 1 1.7E-02 0 0
CUI: C0796028
Disease: ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION
ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION 		1 0 1 1.7E-02 0 0
CUI: C0796124
Disease: Proud Syndrome
Proud Syndrome 		1 0 1 1.7E-02 0 0
CUI: C0796159
Disease: Mental retardation Smith Fineman Myers type
Mental retardation Smith Fineman Myers type 		1 0 1 1.7E-02 0 0
CUI: C1334180
Disease: Inflammatory malignant fibrous histiocytoma
Inflammatory malignant fibrous histiocytoma 		1 0 1 1.7E-02 0 0
CUI: C1334963
Disease: Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma
Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma 		1 0 1 1.7E-02 0 0
CUI: C1368295
Disease: Malignant basal cell tumor
Malignant basal cell tumor 		1 0 1 1.7E-02 0 0
CUI: C1608971
Disease: Optic nerve pallor
Optic nerve pallor 		1 0 1 1.7E-02 0 0
CUI: C1735375
Disease: Progressive optic neuropathy
Progressive optic neuropathy 		1 0 1 1.7E-02 0 0
CUI: C1834038
Disease: Schilbach-Rott Syndrome
Schilbach-Rott Syndrome 		1 0 1 1.7E-02 0 0
CUI: C1834930
Disease: Fusion of the left and right thalami
Fusion of the left and right thalami 		1 0 1 1.7E-02 0 0