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: C0477373
Disease: Other forms of migraine
Other forms of migraine 		2 0 1 0.11 0 0
CUI: C0748071
Disease: psychosocial impairment
psychosocial impairment 		2 0 1 0.11 0 0
CUI: C0856636
Disease: Transient hemiparesis
Transient hemiparesis 		2 0 1 0.11 0 0
CUI: C0949331
Disease: Gonadal Agenesis
Gonadal Agenesis 		2 0 1 0.11 0 0
CUI: C1735856
Disease: Migraine with Typical Aura
Migraine with Typical Aura 		2 0 1 0.11 0 0
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		2 0 1 0.11 0 0
CUI: C1839782
Disease: Macroorchidism, postpubertal
Macroorchidism, postpubertal 		2 0 1 0.11 0 0
CUI: C1846367
Disease: Spinocerebellar ataxia 19
Spinocerebellar ataxia 19 		2 0 1 0.11 0 0
CUI: C1850048
Disease: Absent proximal finger flexion creases
Absent proximal finger flexion creases 		2 0 1 0.11 0 0
CUI: C1856644
Disease: Absent/hypoplastic coccyx
Absent/hypoplastic coccyx 		2 0 1 0.11 0 0
CUI: C1864399
Disease: Peroxisome Biogenesis Disorder, Complementation Group 7
Peroxisome Biogenesis Disorder, Complementation Group 7 		2 0 1 0.11 0 0
CUI: C1865332
Disease: Transient unilateral blurring of vision
Transient unilateral blurring of vision 		2 0 1 0.11 0 0
CUI: C2677843
Disease: Episodic Ataxia, Type 7
Episodic Ataxia, Type 7 		2 0 1 0.11 0 0
CUI: C2678248
Disease: Mood instability
Mood instability 		2 0 1 0.11 0 0
CUI: C2751480
Disease: Hypoplastic coccygeal vertebrae
Hypoplastic coccygeal vertebrae 		2 0 1 0.11 0 0
CUI: C3553660
Disease: Malan overgrowth syndrome
Malan overgrowth syndrome 		2 0 1 0.11 0 0
CUI: C4072884
Disease: Ciliary body coloboma
Ciliary body coloboma 		2 0 1 0.11 0 0
CUI: C0236794
Disease: Panic disorder without agoraphobia
Panic disorder without agoraphobia 		3 0 1 1.0E-01 0 0
CUI: C0270860
Disease: Basilar-Type Migraine
Basilar-Type Migraine 		3 0 1 1.0E-01 0 0
CUI: C0549118
Disease: Hemiplegia-hemiconvulsion-epilepsy syndrome
Hemiplegia-hemiconvulsion-epilepsy syndrome 		3 0 1 1.0E-01 0 0
CUI: C0574080
Disease: Guanidinoacetate methyltransferase deficiency
Guanidinoacetate methyltransferase deficiency 		3 0 1 1.0E-01 0 0
CUI: C0585544
Disease: Downbeat nystagmus
Downbeat nystagmus 		3 0 1 1.0E-01 0 0
CUI: C0701824
Disease: Staggering gait
Staggering gait 		3 0 1 1.0E-01 0 0
CUI: C1364667
Disease: Adrenalitis
Adrenalitis 		3 0 1 1.0E-01 0 0
CUI: C1842073
Disease: Prolonged Electroretinal Response Suppression
Prolonged Electroretinal Response Suppression 		3 0 1 1.0E-01 0 0