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: C0554628
Disease: Group A Streptococcal Infections
Group A Streptococcal Infections
8 0 3 0.14 0 0
CUI: C0342953
Disease: Organ dysfunction syndrome
Organ dysfunction syndrome
17 0 4 0.14 0 0
CUI: C0264964
Disease: Aneurysm of popliteal artery
Aneurysm of popliteal artery
2 0 2 0.12 0 0
CUI: C0270959
Disease: Myotonia Levior
Myotonia Levior
2 0 2 0.12 0 0
CUI: C0751360
Disease: Becker Generalized Myotonia
Becker Generalized Myotonia
2 67 2 0.12 1 1.4E-02
CUI: C1850569
Disease: Nemaline Myopathy 2
Nemaline Myopathy 2
2 265 2 0.12 1 3.7E-03
CUI: C2586331
Disease: Surrogate mother (family issue)
Surrogate mother (family issue)
2 0 2 0.12 0 0
CUI: C2931139
Disease: Nondystrophic myotonia
Nondystrophic myotonia
2 0 2 0.12 0 0
CUI: C4022683
Disease: Myotonia of the upper limb
Myotonia of the upper limb
2 0 2 0.12 0 0
CUI: C1828221
Disease: Non dystrophic myotonia
Non dystrophic myotonia
3 0 2 0.12 0 0
Non-obstructive reflux-associated chronic pyelonephritis (disorder)
13 0 3 0.12 0 0
CUI: C3495566
Disease: Reflux nephropathy (disorder)
Reflux nephropathy (disorder)
13 0 3 0.12 0 0
CUI: C0015634
Disease: Farmer's Lung
Farmer's Lung
4 0 2 0.11 0 0
CUI: C0238357
Disease: Hyperkalemic periodic paralysis
Hyperkalemic periodic paralysis
4 30 2 0.11 1 2.9E-02
CUI: C0264394
Disease: Paraseptal emphysema
Paraseptal emphysema
4 0 2 0.11 0 0
CUI: C0339165
Disease: Perennial allergic conjunctivitis
Perennial allergic conjunctivitis
4 0 2 0.11 0 0
CUI: C1868623
Disease: Handgrip myotonia
Handgrip myotonia
4 0 2 0.11 0 0
CUI: C4022169
Disease: EMG: myotonic discharges
EMG: myotonic discharges
4 3 2 0.11 1 0.14
Calcium Pyrophosphate Dihydrate Deposition
5 0 2 0.11 0 0
CUI: C0524610
Disease: Chronic Alcoholic Hepatitis
Chronic Alcoholic Hepatitis
5 0 2 0.11 0 0
CUI: C0751359
Disease: Percussion Myotonia
Percussion Myotonia
5 0 2 0.11 0 0
CUI: C0009197
Disease: Cochlear Diseases
Cochlear Diseases
6 0 2 1.0E-01 0 0
CUI: C0221055
Disease: Paramyotonia Congenita (disorder)
Paramyotonia Congenita (disorder)
17 26 3 1.0E-01 1 3.3E-02
CUI: C0221763
Disease: Chronic cystitis
Chronic cystitis
6 0 2 1.0E-01 0 0
CUI: C0396060
Disease: Congenital laryngeal adductor palsy
Congenital laryngeal adductor palsy
17 0 3 1.0E-01 0 0