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: C0152236
Disease: Talipes valgus
Talipes valgus 		2 0 1 0.50 0 0
CUI: C0040524
Disease: Septic Toxemia
Septic Toxemia 		4 0 1 0.25 0 0
CUI: C0085700
Disease: Chondromalacia
Chondromalacia 		8 0 1 0.12 0 0
CUI: C1865304
Disease: Overfolding of the superior helices
Overfolding of the superior helices 		10 0 1 1.0E-01 0 0
CUI: C0752210
Disease: Dyskinesias, Paroxysmal
Dyskinesias, Paroxysmal 		15 0 1 6.7E-02 0 0
CUI: C1836392
Disease: Dysmetric saccades
Dysmetric saccades 		18 0 1 5.6E-02 0 0
CUI: C0239882
Disease: Head tremor
Head tremor 		21 0 1 4.8E-02 0 0
CUI: C3894553
Disease: response to simvastatin
response to simvastatin 		21 0 1 4.8E-02 0 0
CUI: C0007302
Disease: Cartilage Diseases
Cartilage Diseases 		23 0 1 4.3E-02 0 0
CUI: C1842587
Disease: Sensory axonal neuropathy
Sensory axonal neuropathy 		23 0 1 4.3E-02 0 0
CUI: C2673410
Disease: Small midface
Small midface 		23 0 1 4.3E-02 0 0
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green 		24 0 1 4.2E-02 0 0
CUI: C1837458
Disease: Impaired smooth pursuit
Impaired smooth pursuit 		25 0 1 4.0E-02 0 0
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia 		26 0 1 3.8E-02 0 0
CUI: C0271390
Disease: Nystagmus, End-Position
Nystagmus, End-Position 		26 0 1 3.8E-02 0 0
CUI: C1704375
Disease: Hypophosphatemic Rickets
Hypophosphatemic Rickets 		29 0 1 3.4E-02 0 0
CUI: C1836996
Disease: Disproportionate tall stature
Disproportionate tall stature 		30 0 1 3.3E-02 0 0
CUI: C0239842
Disease: Tremor of hands
Tremor of hands 		31 0 1 3.2E-02 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 1 3.2E-02 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense 		33 0 1 3.0E-02 0 0
CUI: C1720189
Disease: Episodic Ataxia
Episodic Ataxia 		36 0 1 2.8E-02 0 0
CUI: C1842060
Disease: Prominent supraorbital ridges
Prominent supraorbital ridges 		41 0 1 2.4E-02 0 0
CUI: C0085623
Disease: Akinesia
Akinesia 		43 0 1 2.3E-02 0 0
CUI: C0234144
Disease: Dysgraphia
Dysgraphia 		43 0 1 2.3E-02 0 0
CUI: C3536983
Disease: Familial Hypophosphatemic Rickets
Familial Hypophosphatemic Rickets 		43 0 1 2.3E-02 0 0