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: C1834696
Disease: Hyporeflexia of lower limbs
Hyporeflexia of lower limbs 		19 0 1 5.3E-02 0 0
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		21 24 1 4.8E-02 1 1.6E-02
CUI: C1578482
Disease: Valgus deformities of feet
Valgus deformities of feet 		26 0 1 3.8E-02 0 0
CUI: C1836451
Disease: Distal lower limb amyotrophy
Distal lower limb amyotrophy 		29 0 1 3.4E-02 0 0
CUI: C1866010
Disease: Proximal muscle weakness in lower limbs
Proximal muscle weakness in lower limbs 		30 0 1 3.3E-02 0 0
CUI: C0004031
Disease: Aspergillosis, Allergic Bronchopulmonary
Aspergillosis, Allergic Bronchopulmonary 		31 0 1 3.2E-02 0 0
CUI: C0751336
Disease: Distal Muscular Dystrophies
Distal Muscular Dystrophies 		31 18 1 3.2E-02 1 1.8E-02
CUI: C1850830
Disease: Exercise-induced myalgia
Exercise-induced myalgia 		37 0 1 2.7E-02 0 0
CUI: C0560346
Disease: Difficulty running
Difficulty running 		38 0 1 2.6E-02 0 0
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		41 30 1 2.4E-02 1 1.5E-02
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting 		43 0 1 2.3E-02 0 0
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss 		44 0 1 2.3E-02 0 0
CUI: C0427055
Disease: Facial Paresis
Facial Paresis 		44 0 1 2.3E-02 0 0
CUI: C0004030
Disease: Aspergillosis
Aspergillosis 		47 0 1 2.1E-02 0 0
CUI: C1836450
Disease: Distal lower limb muscle weakness
Distal lower limb muscle weakness 		49 0 1 2.0E-02 0 0
CUI: C3714542
Disease: Lymphoma, Diffuse
Lymphoma, Diffuse 		49 0 1 2.0E-02 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 0 1 2.0E-02 0 0
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		56 0 1 1.8E-02 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		57 0 1 1.8E-02 0 0
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		61 0 1 1.6E-02 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 10 1 1.6E-02 1 2.1E-02
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases 		66 0 1 1.5E-02 0 0
CUI: C0022283
Disease: Incontinentia Pigmenti Achromians
Incontinentia Pigmenti Achromians 		67 0 1 1.5E-02 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		70 0 1 1.4E-02 0 0
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent 		73 0 1 1.4E-02 0 0