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: C0027073
Disease: Myofascial Pain Syndromes
Myofascial Pain Syndromes 		5 0 1 1.0E-01 0 0
CUI: C0086405
Disease: Hereditary Sensory Radicular Neuropathy
Hereditary Sensory Radicular Neuropathy 		5 0 2 0.22 0 0
CUI: C0268849
Disease: Overactive Detrusor
Overactive Detrusor 		5 0 1 1.0E-01 0 0
CUI: C0741548
Disease: bladder symptoms
bladder symptoms 		5 0 1 1.0E-01 0 0
CUI: C1868702
Disease: Diabetic keratopathy
Diabetic keratopathy 		5 0 1 1.0E-01 0 0
CUI: C4021578
Disease: Chronic axonal neuropathy
Chronic axonal neuropathy 		5 0 1 1.0E-01 0 0
CUI: C4049342
Disease: Foot osteomyelitis
Foot osteomyelitis 		5 0 2 0.22 0 0
CUI: C0231791
Disease: Toeing-in
Toeing-in 		6 0 1 9.1E-02 0 0
CUI: C0236000
Disease: Jaw pain
Jaw pain 		6 0 1 9.1E-02 0 0
CUI: C0406670
Disease: Vulvodynia
Vulvodynia 		6 0 1 9.1E-02 0 0
CUI: C0410204
Disease: Myopathy, Centronuclear, Autosomal Recessive
Myopathy, Centronuclear, Autosomal Recessive 		6 0 1 9.1E-02 0 0
CUI: C0546476
Disease: Multiple self-healing squamous epithelioma
Multiple self-healing squamous epithelioma 		6 0 1 9.1E-02 0 0
CUI: C0579144
Disease: Cavovarus deformity of foot
Cavovarus deformity of foot 		6 0 1 9.1E-02 0 0
CUI: C0796037
Disease: Martsolf syndrome
Martsolf syndrome 		6 0 1 9.1E-02 0 0
CUI: C1262037
Disease: Diabetic cystopathy
Diabetic cystopathy 		6 0 1 9.1E-02 0 0
CUI: C4479708
Disease: FCD IIA
FCD IIA 		6 0 1 9.1E-02 0 0
CUI: C0020075
Disease: Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 5 		7 0 1 8.3E-02 0 0
CUI: C0238015
Disease: Autonomic Dysreflexia
Autonomic Dysreflexia 		7 0 1 8.3E-02 0 0
CUI: C0339296
Disease: Neurotrophic keratitis
Neurotrophic keratitis 		7 0 1 8.3E-02 0 0
CUI: C2733564
Disease: Full thickness hole of macula lutea
Full thickness hole of macula lutea 		7 0 1 8.3E-02 0 0
CUI: C0020072
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 2 		8 0 1 7.7E-02 0 0
CUI: C0231531
Disease: Muscle fibrillation
Muscle fibrillation 		8 0 1 7.7E-02 0 0
CUI: C0265233
Disease: Cryptophthalmos syndrome
Cryptophthalmos syndrome 		8 0 1 7.7E-02 0 0
CUI: C1707516
Disease: Corneal Sensitivity
Corneal Sensitivity 		8 0 1 7.7E-02 0 0
CUI: C1723764
Disease: Chronic Prostatitis with Chronic Pelvic Pain Syndrome
Chronic Prostatitis with Chronic Pelvic Pain Syndrome 		8 0 1 7.7E-02 0 0