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: C3671887
Disease: Hypernatriuria
Hypernatriuria
17 0 4 6.9E-02 0 0
CUI: C0342546
Disease: Premature adrenarche
Premature adrenarche
18 0 4 6.8E-02 0 0
CUI: C4021972
Disease: Urogenital sinus anomaly
Urogenital sinus anomaly
18 0 4 6.8E-02 0 0
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism
50 0 6 6.7E-02 0 0
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism
178 0 14 6.7E-02 0 0
CUI: C0268418
Disease: Deficiency of glycerol kinase
Deficiency of glycerol kinase
3 0 3 6.7E-02 0 0
CUI: C0795887
Disease: Complex Glycerol Kinase Deficiency
Complex Glycerol Kinase Deficiency
3 0 3 6.7E-02 0 0
CUI: C0342549
Disease: Familial Testotoxicosis
Familial Testotoxicosis
20 0 4 6.6E-02 0 0
CUI: C0278110
Disease: Hemiplegia, Crossed
Hemiplegia, Crossed
5 2 3 6.4E-02 2 0.15
CUI: C1865322
Disease: MIGRAINE, FAMILIAL HEMIPLEGIC, 2
MIGRAINE, FAMILIAL HEMIPLEGIC, 2
6 0 3 6.2E-02 0 0
CUI: C0020625
Disease: Hyponatremia
Hyponatremia
109 0 9 6.2E-02 0 0
CUI: C0018991
Disease: Hemiplegia
Hemiplegia
41 6 5 6.2E-02 2 0.12
CUI: C0268505
Disease: Ocular albinism, type II
Ocular albinism, type II
7 0 3 6.1E-02 0 0
CUI: C0001624
Disease: Adrenal Gland Neoplasms
Adrenal Gland Neoplasms
94 0 8 6.1E-02 0 0
Hypogonadism, Isolated Hypogonadotropic
42 0 5 6.1E-02 0 0
CUI: C4024878
Disease: Generalized hyperpigmentation
Generalized hyperpigmentation
42 0 5 6.1E-02 0 0
CUI: C0221163
Disease: Motor Disorders
Motor Disorders
25 0 4 6.1E-02 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female
25 0 4 6.1E-02 0 0
Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies
8 0 3 6.0E-02 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases
9 0 3 5.9E-02 0 0
CUI: C0019100
Disease: Severe Dengue
Severe Dengue
117 25 9 5.9E-02 2 5.6E-02
CUI: C4054695
Disease: Familial glucocorticoid deficiency
Familial glucocorticoid deficiency
9 0 3 5.9E-02 0 0
CUI: C0393703
Disease: Myoclonic Absence Epilepsy
Myoclonic Absence Epilepsy
10 0 3 5.8E-02 0 0
CUI: C4049431
Disease: Chronic hepatitis C genotype 4
Chronic hepatitis C genotype 4
10 3 3 5.8E-02 2 0.14
CUI: C0520463
Disease: Chronic active hepatitis
Chronic active hepatitis
122 0 9 5.7E-02 0 0