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 8.6E-03
CUI: C0268958
Disease: Acute orchitis
Acute orchitis 		0 1 0 0 1 8.6E-03
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania 		0 1 0 0 1 8.6E-03
CUI: C0432230
Disease: Langer Mesomelic Dysplasia Syndrome
Langer Mesomelic Dysplasia Syndrome 		0 4 0 0 1 8.4E-03
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		0 17 0 0 1 7.6E-03
CUI: C0877781
Disease: Hemicrania
Hemicrania 		0 1 0 0 1 8.6E-03
CUI: C2585575
Disease: Recurrent abdominal pain
Recurrent abdominal pain 		0 2 0 0 1 8.5E-03
CUI: C3806402
Disease: EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION 		0 38 0 0 1 6.5E-03
CUI: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms 		1 0 1 1.6E-02 0 0
CUI: C0025467
Disease: Mesenteric Cyst
Mesenteric Cyst 		1 2 1 1.6E-02 2 1.7E-02
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma 		1 0 1 1.6E-02 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 1.6E-02 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 1 1 1.6E-02 1 8.6E-03
CUI: C0153470
Disease: Malignant neoplasm of spleen
Malignant neoplasm of spleen 		1 0 1 1.6E-02 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 0 1 1.6E-02 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 0 1 1.6E-02 0 0
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle 		1 0 1 1.6E-02 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 1.6E-02 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 1.6E-02 0 0
CUI: C0206619
Disease: Lymphatic Vessel Tumors
Lymphatic Vessel Tumors 		1 2 1 1.6E-02 2 1.7E-02
CUI: C0220690
Disease: Macrocephaly, benign familial
Macrocephaly, benign familial 		1 0 1 1.6E-02 0 0
CUI: C0232180
Disease: Cardiac shunt
Cardiac shunt 		1 2 1 1.6E-02 2 1.7E-02
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 1.6E-02 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome 		1 0 1 1.6E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 1.6E-02 0 0