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: C1865926
Disease: Infantile convulsions and paroxysmal choreoathetosis, familial (disorder)
Infantile convulsions and paroxysmal choreoathetosis, familial (disorder) 		4 0 3 0.43 0 0
CUI: C4021885
Disease: Atrial cardiomyopathy
Atrial cardiomyopathy 		7 0 3 0.30 0 0
CUI: C0332886
Disease: Coarctation
Coarctation 		8 0 3 0.27 0 0
CUI: C1333500
Disease: Extragastrointestinal Gastrointestinal Stromal Tumor
Extragastrointestinal Gastrointestinal Stromal Tumor 		12 0 3 0.20 0 0
CUI: C3888552
Disease: Autoimmune colitis
Autoimmune colitis 		12 0 3 0.20 0 0
CUI: C0238014
Disease: Acute cerebellar ataxia
Acute cerebellar ataxia 		1 0 1 0.17 0 0
CUI: C0342750
Disease: Glycogen storage disease type Id
Glycogen storage disease type Id 		1 0 1 0.17 0 0
CUI: C1719788
Disease: Episodic ataxia type 1
Episodic ataxia type 1 		16 0 3 0.16 0 0
CUI: C4085595
Disease: AL-RAQAD SYNDROME
AL-RAQAD SYNDROME 		17 0 3 0.15 0 0
CUI: C0544645
Disease: Focal Sensory Seizure
Focal Sensory Seizure 		2 0 1 0.14 0 0
CUI: C1322252
Disease: Chordoid Glioma of the Third Ventricle
Chordoid Glioma of the Third Ventricle 		2 0 1 0.14 0 0
CUI: C2932666
Disease: Gestational Diabetes Insipidus
Gestational Diabetes Insipidus 		2 0 1 0.14 0 0
CUI: C2985174
Disease: Papillary glioneuronal tumor
Papillary glioneuronal tumor 		2 0 1 0.14 0 0
CUI: C0015745
Disease: Feeding behaviors
Feeding behaviors 		3 0 1 0.12 0 0
CUI: C0267176
Disease: Gastroparesis with diabetes mellitus
Gastroparesis with diabetes mellitus 		21 0 3 0.12 0 0
CUI: C0268443
Disease: Acquired Nephrogenic Diabetes Insipidus
Acquired Nephrogenic Diabetes Insipidus 		3 0 1 0.12 0 0
CUI: C0342311
Disease: Neuroglycopenia
Neuroglycopenia 		3 0 1 0.12 0 0
CUI: C1563706
Disease: Nephrogenic Diabetes Insipidus, Type II
Nephrogenic Diabetes Insipidus, Type II 		3 0 1 0.12 0 0
CUI: C1853995
Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 2
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 		3 0 1 0.12 0 0
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		21 0 3 0.12 0 0
CUI: C3542500
Disease: ADH-Resistant Diabetes Insipidus
ADH-Resistant Diabetes Insipidus 		3 0 1 0.12 0 0
CUI: C2827362
Disease: Myeloid/Lymphoid Neoplasms with FGFR1 Rearrangement
Myeloid/Lymphoid Neoplasms with FGFR1 Rearrangement 		22 0 3 0.12 0 0
CUI: C3495488
Disease: Axenfeld-Rieger syndrome
Axenfeld-Rieger syndrome 		22 0 3 0.12 0 0
CUI: C0853104
Disease: Renal tubular atrophy
Renal tubular atrophy 		4 0 1 0.11 0 0
CUI: C1302746
Disease: Melanocytic neoplasm
Melanocytic neoplasm 		4 0 1 0.11 0 0