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: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 0.50 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 0.50 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 0.50 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 0.50 0 0
CUI: C1865241
Disease: Large sternal ossification centers
Large sternal ossification centers 		1 0 1 0.50 0 0
CUI: C1865254
Disease: Distal widening of metacarpals
Distal widening of metacarpals 		1 0 1 0.50 0 0
CUI: C3494934
Disease: Benign paroxysmal torticollis of infancy
Benign paroxysmal torticollis of infancy 		1 0 1 0.50 0 0
CUI: C4016713
Disease: EPISODIC ATAXIA, TYPE 2, AND EPILEPSY
EPISODIC ATAXIA, TYPE 2, AND EPILEPSY 		1 0 1 0.50 0 0
CUI: C4021571
Disease: Abnormal vestibulo-ocular reflex
Abnormal vestibulo-ocular reflex 		1 0 1 0.50 0 0
CUI: C4024187
Disease: Bullet-shaped middle phalanges of the hand
Bullet-shaped middle phalanges of the hand 		1 0 1 0.50 0 0
CUI: C4310716
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42 		1 0 1 0.50 0 0
CUI: C0265211
Disease: Marshall-Smith syndrome
Marshall-Smith syndrome 		2 17 1 0.33 4 0.17
CUI: C0477373
Disease: Other forms of migraine
Other forms of migraine 		2 0 1 0.33 0 0
CUI: C0856636
Disease: Transient hemiparesis
Transient hemiparesis 		2 0 1 0.33 0 0
CUI: C1735856
Disease: Migraine with Typical Aura
Migraine with Typical Aura 		2 0 1 0.33 0 0
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		2 0 1 0.33 0 0
CUI: C1833145
Disease: Distal ulnar hypoplasia
Distal ulnar hypoplasia 		2 0 1 0.33 0 0
CUI: C1841648
Disease: Short mandibular rami
Short mandibular rami 		2 0 1 0.33 0 0
CUI: C1846367
Disease: Spinocerebellar ataxia 19
Spinocerebellar ataxia 19 		2 0 1 0.33 0 0
CUI: C1865332
Disease: Transient unilateral blurring of vision
Transient unilateral blurring of vision 		2 0 1 0.33 0 0
CUI: C2677843
Disease: Episodic Ataxia, Type 7
Episodic Ataxia, Type 7 		2 0 1 0.33 0 0
CUI: C0270860
Disease: Basilar-Type Migraine
Basilar-Type Migraine 		3 0 1 0.25 0 0
CUI: C0549118
Disease: Hemiplegia-hemiconvulsion-epilepsy syndrome
Hemiplegia-hemiconvulsion-epilepsy syndrome 		3 0 1 0.25 0 0
CUI: C0585544
Disease: Downbeat nystagmus
Downbeat nystagmus 		3 0 1 0.25 0 0
CUI: C0701824
Disease: Staggering gait
Staggering gait 		3 0 1 0.25 0 0