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: C4304347
Disease: Timothy syndrome type 2
Timothy syndrome type 2 		0 4 0 0 2 7.1E-02
CUI: C4703722
Disease: Superior rectus muscle underaction
Superior rectus muscle underaction 		0 1 0 0 1 3.8E-02
CUI: C0010334
Disease: Crisscross Heart
Crisscross Heart 		1 0 1 7.9E-03 0 0
CUI: C0024954
Disease: Maxillary Neoplasms
Maxillary Neoplasms 		1 0 1 7.9E-03 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 7.9E-03 0 0
CUI: C0040409
Disease: Tongue Diseases
Tongue Diseases 		1 0 1 7.9E-03 0 0
CUI: C0042818
Disease: Visual discomfort
Visual discomfort 		1 0 1 7.9E-03 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 7.9E-03 0 0
CUI: C0154863
Disease: Vitreoretinal dystrophy
Vitreoretinal dystrophy 		1 0 1 7.9E-03 0 0
CUI: C0155411
Disease: Exostosis of external ear canal
Exostosis of external ear canal 		1 0 1 7.9E-03 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 0 1 7.9E-03 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 0 1 7.9E-03 0 0
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle 		1 0 1 7.9E-03 0 0
CUI: C0206649
Disease: Neoplasms, Fibroepithelial
Neoplasms, Fibroepithelial 		1 0 1 7.9E-03 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 7.9E-03 0 0
CUI: C0231246
Disease: Failure to gain weight
Failure to gain weight 		1 0 1 7.9E-03 0 0
CUI: C0231450
Disease: Abnormal extension
Abnormal extension 		1 0 1 7.9E-03 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 7.9E-03 0 0
CUI: C0232308
Disease: P pulmonale by EKG (finding)
P pulmonale by EKG (finding) 		1 0 1 7.9E-03 0 0
CUI: C0241633
Disease: Vaginal dryness
Vaginal dryness 		1 0 1 7.9E-03 0 0
CUI: C0264963
Disease: Aneurysm of femoral artery
Aneurysm of femoral artery 		1 0 1 7.9E-03 0 0
CUI: C0265257
Disease: Genee-Wiedemann syndrome
Genee-Wiedemann syndrome 		1 0 1 7.9E-03 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 7.9E-03 0 0
CUI: C0265573
Disease: Phocomelia of upper limb
Phocomelia of upper limb 		1 0 1 7.9E-03 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 7.9E-03 0 0