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: C1527366
Disease: Salaam Seizures
Salaam Seizures 		75 0 1 2.6E-03 0 0
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia 		75 0 1 2.6E-03 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin 		75 0 1 2.6E-03 0 0
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy 		74 0 1 2.6E-03 0 0
CUI: C3554617
Disease: Adducted thumb
Adducted thumb 		74 0 1 2.6E-03 0 0
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		73 0 1 2.6E-03 0 0
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent 		73 0 1 2.6E-03 0 0
CUI: C0011226
Disease: Hepatitis D Infection
Hepatitis D Infection 		72 0 1 2.6E-03 0 0
CUI: C0035579
Disease: Rickets
Rickets 		72 0 1 2.6E-03 0 0
CUI: C1844813
Disease: Widely spaced teeth
Widely spaced teeth 		71 0 1 2.6E-03 0 0
CUI: C0426415
Disease: Large nose
Large nose 		70 0 1 2.6E-03 0 0
CUI: C0542514
Disease: Blue sclera
Blue sclera 		70 0 1 2.6E-03 0 0
CUI: C0020620
Disease: Hypohidrosis
Hypohidrosis 		69 0 1 2.6E-03 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		68 0 1 2.6E-03 0 0
CUI: C0562350
Disease: Hip circumference
Hip circumference 		68 0 1 2.6E-03 0 0
CUI: C4282407
Disease: Sparse and thin eyebrow
Sparse and thin eyebrow 		68 0 1 2.6E-03 0 0
CUI: C0266491
Disease: Neuronal heterotopia
Neuronal heterotopia 		67 0 1 2.6E-03 0 0
CUI: C1285498
Disease: Vegetation
Vegetation 		67 0 1 2.6E-03 0 0
CUI: C1850456
Disease: Progressive microcephaly
Progressive microcephaly 		67 0 1 2.6E-03 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		66 0 1 2.7E-03 0 0
CUI: C3501844
Disease: Familial Nonmedullary Thyroid Cancer
Familial Nonmedullary Thyroid Cancer 		66 0 1 2.7E-03 0 0
CUI: C0948192
Disease: Primary infection NOS
Primary infection NOS 		65 0 1 2.7E-03 0 0
CUI: C1837108
Disease: Decreased muscle mass
Decreased muscle mass 		65 0 1 2.7E-03 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 1 2.7E-03 0 0
CUI: C0973461
Disease: Dysphasia
Dysphasia 		63 0 1 2.7E-03 0 0