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: C0010334
Disease: Crisscross Heart
Crisscross Heart 		1 0 1 5.3E-03 0 0
CUI: C0027063
Disease: Myoclonic disorder
Myoclonic disorder 		1 0 1 5.3E-03 0 0
CUI: C0029307
Disease: Oroya Fever
Oroya Fever 		1 0 1 5.3E-03 0 0
CUI: C0034350
Disease: Pyruvate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors 		1 0 1 5.3E-03 0 0
CUI: C0038834
Disease: Superior Vena Cava Thrombosis
Superior Vena Cava Thrombosis 		1 0 1 5.3E-03 0 0
CUI: C0155002
Disease: Sudden visual loss
Sudden visual loss 		1 0 1 5.3E-03 0 0
CUI: C0220690
Disease: Macrocephaly, benign familial
Macrocephaly, benign familial 		1 0 1 5.3E-03 0 0
CUI: C0221069
Disease: Anterior Spinal Artery Syndrome
Anterior Spinal Artery Syndrome 		1 0 1 5.3E-03 0 0
CUI: C0221151
Disease: Projectile vomiting
Projectile vomiting 		1 0 1 5.3E-03 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 5.3E-03 0 0
CUI: C0232910
Disease: Teratogenesis
Teratogenesis 		1 0 1 5.3E-03 0 0
CUI: C0234458
Disease: Dream disorder
Dream disorder 		1 0 1 5.3E-03 0 0
CUI: C0235584
Disease: Granulocytopenia severe
Granulocytopenia severe 		1 0 1 5.3E-03 0 0
CUI: C0235909
Disease: Impaired psychomotor development
Impaired psychomotor development 		1 0 1 5.3E-03 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 5.3E-03 0 0
CUI: C0264954
Disease: Arteriovascular degeneration
Arteriovascular degeneration 		1 0 1 5.3E-03 0 0
CUI: C0265201
Disease: De Sanctis-Cacchione syndrome
De Sanctis-Cacchione syndrome 		1 0 1 5.3E-03 0 0
CUI: C0265988
Disease: Congenital accessory skin tag
Congenital accessory skin tag 		1 0 1 5.3E-03 0 0
CUI: C0266507
Disease: Myeloschisis
Myeloschisis 		1 0 1 5.3E-03 0 0
CUI: C0268262
Disease: Metachromatic Leukodystrophy due to Saposin B Deficiency
Metachromatic Leukodystrophy due to Saposin B Deficiency 		1 0 1 5.3E-03 0 0
CUI: C0268500
Disease: Yellow mutant oculocutaneous albinism
Yellow mutant oculocutaneous albinism 		1 0 1 5.3E-03 0 0
CUI: C0270627
Disease: Myelitis, Acute Transverse
Myelitis, Acute Transverse 		1 0 1 5.3E-03 0 0
CUI: C0272263
Disease: Cryofibrinogenemia
Cryofibrinogenemia 		1 0 1 5.3E-03 0 0
CUI: C0275584
Disease: Cutaneous nocardiosis
Cutaneous nocardiosis 		1 0 1 5.3E-03 0 0
CUI: C0281334
Disease: Adult Papillary Meningioma
Adult Papillary Meningioma 		1 0 1 5.3E-03 0 0