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: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome 		185 0 29 0.12 0 0
CUI: C0085395
Disease: Ureaplasma Infections
Ureaplasma Infections 		12 0 10 0.10 0 0
CUI: C0332447
Disease: Morphologically abnormal structure (morphologic abnormality)
Morphologically abnormal structure (morphologic abnormality) 		20 0 10 9.6E-02 0 0
CUI: C0023092
Disease: Lassa Fever
Lassa Fever 		22 0 10 9.4E-02 0 0
CUI: C0919909
Disease: Tonic clonic movements
Tonic clonic movements 		22 0 10 9.4E-02 0 0
CUI: C1859726
Disease: ARTERIAL TORTUOSITY SYNDROME
ARTERIAL TORTUOSITY SYNDROME 		37 0 11 9.2E-02 0 0
CUI: C0019104
Disease: Hemorrhagic Fevers, Viral
Hemorrhagic Fevers, Viral 		57 0 12 8.6E-02 0 0
CUI: C0206093
Disease: Neuroectodermal Tumors
Neuroectodermal Tumors 		56 0 11 7.9E-02 0 0
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		56 0 10 7.1E-02 0 0
CUI: C0086237
Disease: Epilepsy, Cryptogenic
Epilepsy, Cryptogenic 		88 0 12 7.1E-02 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		89 0 12 7.0E-02 0 0
CUI: C1853237
Disease: Isolated cases
Isolated cases 		111 0 13 6.8E-02 0 0
CUI: C0236018
Disease: Aura
Aura 		83 0 11 6.6E-02 0 0
CUI: C0751111
Disease: Awakening Epilepsy
Awakening Epilepsy 		83 0 11 6.6E-02 0 0
CUI: C0683322
Disease: Mental impairment
Mental impairment 		67 0 10 6.6E-02 0 0
CUI: C0262587
Disease: Parathyroid Adenoma
Parathyroid Adenoma 		133 0 14 6.6E-02 0 0
CUI: C3711376
Disease: Isodicentric Chromosome 15 Syndrome
Isodicentric Chromosome 15 Syndrome 		39 0 8 6.4E-02 0 0
CUI: C0020502
Disease: Hyperparathyroidism
Hyperparathyroidism 		111 0 12 6.2E-02 0 0
CUI: C3203358
Disease: Hypoventilation
Hypoventilation 		28 0 7 6.1E-02 0 0
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		328 0 24 6.0E-02 0 0
CUI: C0242510
Disease: Drug usage
Drug usage 		170 0 15 6.0E-02 0 0
CUI: C1386091
Disease: Acromicria
Acromicria 		13 0 6 5.9E-02 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance 		211 0 17 5.9E-02 0 0
CUI: C1535926
Disease: Neurodevelopmental Disorders
Neurodevelopmental Disorders 		535 0 35 5.9E-02 0 0
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		234 368 18 5.8E-02 8 1.6E-02