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: C0018051
Disease: Gonadal Dysgenesis
Gonadal Dysgenesis 		53 6 30 0.16 6 0.29
CUI: C0242526
Disease: Gonadal Dysgenesis, 45,X
Gonadal Dysgenesis, 45,X 		23 0 23 0.14 0 0
CUI: C0271561
Disease: Somatotropin deficiency
Somatotropin deficiency 		154 14 33 0.12 2 6.1E-02
CUI: C0432474
Disease: Klinefelter's syndrome - male with more than two X chromosomes
Klinefelter's syndrome - male with more than two X chromosomes 		90 5 24 0.11 1 4.0E-02
CUI: C0022735
Disease: Klinefelter Syndrome
Klinefelter Syndrome 		150 18 29 0.10 1 2.6E-02
CUI: C2930619
Disease: Sex Differentiation Disorders
Sex Differentiation Disorders 		103 0 23 9.5E-02 0 0
CUI: C0520463
Disease: Chronic active hepatitis
Chronic active hepatitis 		122 0 24 9.2E-02 0 0
CUI: C0232939
Disease: Primary physiologic amenorrhea
Primary physiologic amenorrhea 		129 0 24 9.0E-02 0 0
CUI: C0206081
Disease: Hyperandrogenism
Hyperandrogenism 		108 0 22 8.9E-02 0 0
CUI: C0266362
Disease: Ambiguous Genitalia
Ambiguous Genitalia 		109 0 22 8.8E-02 0 0
CUI: C0014130
Disease: Endocrine System Diseases
Endocrine System Diseases 		74 0 19 8.8E-02 0 0
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		178 0 27 8.6E-02 0 0
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency 		168 0 26 8.6E-02 0 0
CUI: C0016053
Disease: Fibromyalgia
Fibromyalgia 		143 38 24 8.5E-02 1 1.7E-02
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
46, XY Disorders of Sex Development 		29 0 15 8.5E-02 0 0
CUI: C0206661
Disease: Gonadoblastoma
Gonadoblastoma 		34 0 15 8.3E-02 0 0
CUI: C0020550
Disease: Hyperthyroidism
Hyperthyroidism 		279 27 33 8.1E-02 1 2.1E-02
CUI: C0852036
Disease: Pregnancy associated hypertension
Pregnancy associated hypertension 		186 43 26 8.1E-02 2 3.2E-02
CUI: C0948896
Disease: Primary hypogonadism
Primary hypogonadism 		80 0 18 8.0E-02 0 0
CUI: C0018054
Disease: Gonadal Dysgenesis, 46,XY
Gonadal Dysgenesis, 46,XY 		29 0 14 7.9E-02 0 0
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		335 131 36 7.8E-02 2 1.3E-02
CUI: C0432475
Disease: XX males
XX males 		32 0 14 7.8E-02 0 0
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases 		230 26 28 7.7E-02 3 6.8E-02
CUI: C4552766
Disease: Miscarriage
Miscarriage 		426 56 42 7.7E-02 3 4.1E-02
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		161 76 23 7.7E-02 2 2.1E-02