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: C0007787
Disease: Transient Ischemic Attack
Transient Ischemic Attack 		0 16 0 0 1 1.9E-02
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 1.0E-01 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 1.0E-01 0 0
CUI: C0266284
Disease: Lingual Thyroid
Lingual Thyroid 		1 0 1 1.0E-01 0 0
CUI: C0271285
Disease: Epithelial basement membrane dystrophy
Epithelial basement membrane dystrophy 		1 0 1 1.0E-01 0 0
CUI: C0334689
Disease: C cell tumor
C cell tumor 		1 0 1 1.0E-01 0 0
CUI: C0338483
Disease: Migraine with Prolonged Aura
Migraine with Prolonged Aura 		1 0 1 1.0E-01 0 0
CUI: C0339271
Disease: Salzmann nodular dystrophy
Salzmann nodular dystrophy 		1 0 1 1.0E-01 0 0
CUI: C0342844
Disease: Disorder of glycoprotein metabolism
Disorder of glycoprotein metabolism 		1 0 1 1.0E-01 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 1.0E-01 0 0
CUI: C0521723
Disease: Corneal dystrophy, epithelial basement membrane
Corneal dystrophy, epithelial basement membrane 		1 0 1 1.0E-01 0 0
CUI: C0581882
Disease: Transient neurological symptoms
Transient neurological symptoms 		1 0 1 1.0E-01 0 0
CUI: C1262008
Disease: Hyperphosphatasemia
Hyperphosphatasemia 		1 0 1 1.0E-01 0 0
CUI: C1266055
Disease: Mixed medullary-follicular carcinoma
Mixed medullary-follicular carcinoma 		1 0 1 1.0E-01 0 0
CUI: C1266099
Disease: Thyroid Gland Spindle Cell Tumor with Thymus-Like Differentiation
Thyroid Gland Spindle Cell Tumor with Thymus-Like Differentiation 		1 0 1 1.0E-01 0 0
CUI: C1608983
Disease: Mal de debarquement
Mal de debarquement 		1 0 1 1.0E-01 0 0
CUI: C1641846
Disease: Groenouw corneal dystrophy type I (disorder)
Groenouw corneal dystrophy type I (disorder) 		1 0 1 1.0E-01 0 0
CUI: C1709166
Disease: Neoplastic C-Cell Hyperplasia
Neoplastic C-Cell Hyperplasia 		1 0 1 1.0E-01 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 1 1 1.0E-01 1 2.7E-02
CUI: C1837974
Disease: Corneal Dystrophy, Lattice Type IIIA
Corneal Dystrophy, Lattice Type IIIA 		1 0 1 1.0E-01 0 0
CUI: C1865323
Disease: Migraine, Familial Basilar
Migraine, Familial Basilar 		1 1 1 1.0E-01 1 2.7E-02
CUI: C2349460
Disease: Pure menstrual migraine
Pure menstrual migraine 		1 0 1 1.0E-01 0 0
CUI: C3150908
Disease: MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13 		1 0 1 1.0E-01 0 0
CUI: C3264000
Disease: Refractory juvenile myoclonic epilepsy
Refractory juvenile myoclonic epilepsy 		1 0 1 1.0E-01 0 0
CUI: C3494934
Disease: Benign paroxysmal torticollis of infancy
Benign paroxysmal torticollis of infancy 		1 0 1 1.0E-01 0 0