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: C1854181
Disease: FIBROMATOSIS, GINGIVAL, 2
FIBROMATOSIS, GINGIVAL, 2 		6 0 3 0.43 0 0
CUI: C4021885
Disease: Atrial cardiomyopathy
Atrial cardiomyopathy 		7 0 3 0.38 0 0
CUI: C0332886
Disease: Coarctation
Coarctation 		8 0 3 0.33 0 0
CUI: C1843146
Disease: Normal interictal EEG
Normal interictal EEG 		4 0 2 0.33 0 0
CUI: C1851936
Disease: Paroxysmal choreoathetosis
Paroxysmal choreoathetosis 		5 0 2 0.29 0 0
CUI: C0238014
Disease: Acute cerebellar ataxia
Acute cerebellar ataxia 		1 0 1 0.25 0 0
CUI: C0271616
Disease: Precocious female puberty
Precocious female puberty 		1 0 1 0.25 0 0
CUI: C3280415
Disease: COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA
COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA 		1 0 1 0.25 0 0
CUI: C1333500
Disease: Extragastrointestinal Gastrointestinal Stromal Tumor
Extragastrointestinal Gastrointestinal Stromal Tumor 		12 0 3 0.23 0 0
CUI: C3888552
Disease: Autoimmune colitis
Autoimmune colitis 		12 0 3 0.23 0 0
CUI: C0544645
Disease: Focal Sensory Seizure
Focal Sensory Seizure 		2 0 1 0.20 0 0
CUI: C1322252
Disease: Chordoid Glioma of the Third Ventricle
Chordoid Glioma of the Third Ventricle 		2 0 1 0.20 0 0
CUI: C2985174
Disease: Papillary glioneuronal tumor
Papillary glioneuronal tumor 		2 0 1 0.20 0 0
CUI: C3281191
Disease: SCN8A-related epilepsy with encephalopathy
SCN8A-related epilepsy with encephalopathy 		2 0 1 0.20 0 0
CUI: C4023491
Disease: Interictal epileptiform activity
Interictal epileptiform activity 		2 0 1 0.20 0 0
CUI: C4310728
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 5
SEIZURES, BENIGN FAMILIAL INFANTILE, 5 		2 0 1 0.20 0 0
CUI: C1719788
Disease: Episodic ataxia type 1
Episodic ataxia type 1 		16 0 3 0.18 0 0
CUI: C0015745
Disease: Feeding behaviors
Feeding behaviors 		3 0 1 0.17 0 0
CUI: C0037140
Disease: B Virus Infection
B Virus Infection 		3 0 1 0.17 0 0
CUI: C0268443
Disease: Acquired Nephrogenic Diabetes Insipidus
Acquired Nephrogenic Diabetes Insipidus 		3 0 1 0.17 0 0
CUI: C1563706
Disease: Nephrogenic Diabetes Insipidus, Type II
Nephrogenic Diabetes Insipidus, Type II 		3 0 1 0.17 0 0
CUI: C1836829
Disease: Developmental stagnation at onset of seizures
Developmental stagnation at onset of seizures 		3 0 1 0.17 0 0
CUI: C1853995
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 2
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 		3 7 1 0.17 3 0.23
CUI: C1869117
Disease: Paroxysmal nonkinesigenic dyskinesia
Paroxysmal nonkinesigenic dyskinesia 		10 0 2 0.17 0 0
CUI: C3542500
Disease: ADH-Resistant Diabetes Insipidus
ADH-Resistant Diabetes Insipidus 		3 0 1 0.17 0 0