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: C3887992
Disease: THYROTROPIN-RELEASING HORMONE DEFICIENCY
THYROTROPIN-RELEASING HORMONE DEFICIENCY 		1 0 1 0.11 0 0
CUI: C3888911
Disease: CYP2C19 poor metaboliser status
CYP2C19 poor metaboliser status 		1 0 1 0.11 0 0
CUI: C4476780
Disease: Reduced amygdala volume
Reduced amygdala volume 		1 0 1 0.11 0 0
CUI: C0085628
Disease: Stupor
Stupor 		2 0 1 1.0E-01 0 0
CUI: C0270942
Disease: Myasthenic crisis
Myasthenic crisis 		2 0 1 1.0E-01 0 0
CUI: C0392375
Disease: despondency
despondency 		2 0 1 1.0E-01 0 0
CUI: C0393947
Disease: Cholinergic crisis
Cholinergic crisis 		2 0 1 1.0E-01 0 0
CUI: C0728821
Disease: Parasympathomimetic Disorders
Parasympathomimetic Disorders 		2 0 1 1.0E-01 0 0
CUI: C0743073
Disease: depression anxiety disorder
depression anxiety disorder 		2 0 1 1.0E-01 0 0
CUI: C0936243
Disease: HIV-1-Associated Cognitive Motor Complex
HIV-1-Associated Cognitive Motor Complex 		2 0 1 1.0E-01 0 0
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		2 0 1 1.0E-01 0 0
CUI: C1142436
Disease: Sundowning
Sundowning 		2 0 1 1.0E-01 0 0
CUI: C1845248
Disease: Outbursts
Outbursts 		2 0 1 1.0E-01 0 0
CUI: C1845359
Disease: Spinal Muscular Atrophy, Distal, X-Linked 3
Spinal Muscular Atrophy, Distal, X-Linked 3 		2 0 1 1.0E-01 0 0
CUI: C2985307
Disease: Maternal Hypotension
Maternal Hypotension 		2 0 1 1.0E-01 0 0
CUI: C3281191
Disease: SCN8A-related epilepsy with encephalopathy
SCN8A-related epilepsy with encephalopathy 		2 0 1 1.0E-01 0 0
CUI: C3698497
Disease: Axillary web syndrome
Axillary web syndrome 		2 0 1 1.0E-01 0 0
CUI: C4023491
Disease: Interictal epileptiform activity
Interictal epileptiform activity 		2 0 1 1.0E-01 0 0
CUI: C4025031
Disease: Aplasia/hypoplasia of the humerus
Aplasia/hypoplasia of the humerus 		2 0 1 1.0E-01 0 0
CUI: C4025537
Disease: Humerus varus
Humerus varus 		2 0 1 1.0E-01 0 0
CUI: C4055195
Disease: Congenital Isolated Thyroid Stimulating Hormone Deficiency
Congenital Isolated Thyroid Stimulating Hormone Deficiency 		2 0 1 1.0E-01 0 0
CUI: C4310728
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 5
SEIZURES, BENIGN FAMILIAL INFANTILE, 5 		2 0 1 1.0E-01 0 0
CUI: C0005899
Disease: Body Rocking
Body Rocking 		3 0 1 9.1E-02 0 0
CUI: C0027145
Disease: Myxedema
Myxedema 		3 0 1 9.1E-02 0 0
CUI: C0037140
Disease: B Virus Infection
B Virus Infection 		3 0 1 9.1E-02 0 0