Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Duchenne or Becker muscular dystrophy
7 0 3 0.19 0 0
CUI: C1540600
Disease: Cerebral seizure
Cerebral seizure
2 0 2 0.17 0 0
Severe childhood autosomal recessive muscular dystrophy
3 0 2 0.15 0 0
CUI: C0346057
Disease: Cutaneous neurofibroma
Cutaneous neurofibroma
5 0 2 0.13 0 0
Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)
14 0 3 0.13 0 0
CUI: C2945698
Disease: panic symptoms
panic symptoms
6 0 2 0.12 0 0
CUI: C3203509
Disease: Neuropsychiatric syndrome
Neuropsychiatric syndrome
6 0 2 0.12 0 0
CUI: C0013369
Disease: Dysentery
Dysentery
7 0 2 0.12 0 0
CUI: C0154437
Disease: Atypical depressive disorder
Atypical depressive disorder
7 0 2 0.12 0 0
CUI: C1834674
Disease: BETHLEM MYOPATHY 1
BETHLEM MYOPATHY 1
17 0 3 0.12 0 0
CUI: C0014534
Disease: Epididymitis
Epididymitis
8 0 2 0.11 0 0
CUI: C0041471
Disease: TYPHUS
TYPHUS
8 0 2 0.11 0 0
CUI: C0343758
Disease: Typhus group rickettsial disease
Typhus group rickettsial disease
8 0 2 0.11 0 0
CUI: C0035302
Disease: Retinal Artery Occlusion
Retinal Artery Occlusion
9 0 2 0.11 0 0
CUI: C0451819
Disease: Simple obesity
Simple obesity
9 0 2 0.11 0 0
CUI: C2936332
Disease: Alpha-Sarcoglycanopathies
Alpha-Sarcoglycanopathies
9 0 2 0.11 0 0
CUI: C3554225
Disease: LEPTIN RECEPTOR DEFICIENCY
LEPTIN RECEPTOR DEFICIENCY
9 0 2 0.11 0 0
CUI: C4022024
Disease: Upper limb asymmetry
Upper limb asymmetry
9 0 2 0.11 0 0
CUI: C2936331
Disease: Sarcoglycanopathies
Sarcoglycanopathies
20 0 3 0.10 0 0
CUI: C3160844
Disease: PAI-1 polymorphism
PAI-1 polymorphism
10 0 2 1.0E-01 0 0
CUI: C3714976
Disease: ACTIVATED PI3K-DELTA SYNDROME
ACTIVATED PI3K-DELTA SYNDROME
10 0 2 1.0E-01 0 0
CUI: C0162819
Disease: Skin Diseases, Vascular
Skin Diseases, Vascular
11 0 2 9.5E-02 0 0
CUI: C3274592
Disease: Lipofibromatosis
Lipofibromatosis
11 0 2 9.5E-02 0 0
CUI: C0032962
Disease: Pregnancy Complications
Pregnancy Complications
13 0 2 8.7E-02 0 0
CUI: C0152439
Disease: Retinoschisis
Retinoschisis
13 0 2 8.7E-02 0 0