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: 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
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
Chronic Prostatitis with Chronic Pelvic Pain Syndrome
8 0 1 7.7E-02 0 0
CUI: C1837602
Disease: Painless fractures due to injury
Painless fractures due to injury
8 0 1 7.7E-02 0 0
CUI: C1968790
Disease: Axonal degeneration/regeneration
Axonal degeneration/regeneration
8 0 1 7.7E-02 0 0
CUI: C3277059
Disease: Congenital Bilateral Cataracts
Congenital Bilateral Cataracts
8 0 1 7.7E-02 0 0
CUI: C4021222
Disease: Impaired temperature sensation
Impaired temperature sensation
8 0 1 7.7E-02 0 0
CUI: C4025785
Disease: Abnormality of the foot musculature
Abnormality of the foot musculature
8 0 1 7.7E-02 0 0
CUI: C4732740
Disease: Acral ulceration
Acral ulceration
8 0 1 7.7E-02 0 0
CUI: C0011251
Disease: Delusional disorder
Delusional disorder
9 0 1 7.1E-02 0 0
CUI: C0020074
Disease: HSAN Type IV
HSAN Type IV
9 0 1 7.1E-02 0 0
CUI: C1274788
Disease: Atopic keratoconjunctivitis
Atopic keratoconjunctivitis
9 0 1 7.1E-02 0 0
Distal sensory impairment of all modalities
9 0 1 7.1E-02 0 0
CUI: C4020898
Disease: Overactive bladder syndrome
Overactive bladder syndrome
9 0 1 7.1E-02 0 0
CUI: C4025830
Disease: Peripheral axonal degeneration
Peripheral axonal degeneration
9 0 1 7.1E-02 0 0
CUI: C4087506
Disease: Central neuropathic pain
Central neuropathic pain
9 0 1 7.1E-02 0 0
CUI: C0025164
Disease: Megaesophagus
Megaesophagus
10 0 1 6.7E-02 0 0
CUI: C0426359
Disease: Urinary symptoms
Urinary symptoms
10 0 1 6.7E-02 0 0
CUI: C0751117
Disease: Cryptogenic Tonic-Clonic Epilepsy
Cryptogenic Tonic-Clonic Epilepsy
10 0 1 6.7E-02 0 0
CUI: C0751118
Disease: Epilepsy, Tonic-Clonic, Familial
Epilepsy, Tonic-Clonic, Familial
10 0 1 6.7E-02 0 0
CUI: C0751119
Disease: Epilepsy, Tonic-Clonic, Symptomatic
Epilepsy, Tonic-Clonic, Symptomatic
10 0 1 6.7E-02 0 0