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: C0152240
Disease: Uterus bilocularis
Uterus bilocularis
6 0 4 0.20 0 0
CUI: C1698581
Disease: Rokitansky Kuster Hauser syndrome
Rokitansky Kuster Hauser syndrome
27 0 7 0.18 0 0
CUI: C1849930
Disease: Persistent Mullerian duct syndrome
Persistent Mullerian duct syndrome
9 0 3 0.12 0 0
CUI: C0425913
Disease: Uterus absent (finding)
Uterus absent (finding)
10 0 3 0.12 0 0
CUI: C0311357
Disease: ovarian cystic disease
ovarian cystic disease
2 0 2 0.11 0 0
Aplasia/Hypoplasia of metatarsal bones
3 0 2 0.11 0 0
Aplasia/Hypoplasia of the phalanges of the toes
3 0 2 0.11 0 0
Aplasia/Hypoplasia of the phalanges of the hand
4 0 2 1.0E-01 0 0
CUI: C2112532
Disease: Postmenopausal endometrium
Postmenopausal endometrium
15 0 3 1.0E-01 0 0
CUI: C0027086
Disease: Myoma
Myoma
28 0 4 9.5E-02 0 0
Abnormality of male internal genitalia
5 0 2 9.5E-02 0 0
CUI: C0154088
Disease: Carcinoma in situ of prostate
Carcinoma in situ of prostate
6 0 2 9.1E-02 0 0
CUI: C1533568
Disease: fertility disorders
fertility disorders
18 0 3 9.1E-02 0 0
CUI: C0156372
Disease: Asherman Syndrome
Asherman Syndrome
7 0 2 8.7E-02 0 0
CUI: C0264184
Disease: Degenerative spondylolisthesis
Degenerative spondylolisthesis
7 0 2 8.7E-02 0 0
Aplasia/Hypoplasia involving the metacarpal bones
7 0 2 8.7E-02 0 0
Congenital malformation of genital organs
8 0 2 8.3E-02 0 0
CUI: C0334318
Disease: Lipid-rich carcinoma
Lipid-rich carcinoma
8 0 2 8.3E-02 0 0
CUI: C4551490
Disease: Ovotestis
Ovotestis
8 0 2 8.3E-02 0 0
CUI: C0158447
Disease: Idiopathic osteoporosis
Idiopathic osteoporosis
10 0 2 7.7E-02 0 0
CUI: C0431637
Disease: Mullerian aplasia
Mullerian aplasia
10 0 2 7.7E-02 0 0
CUI: C0746025
Disease: Lumbar spondylolisthesis
Lumbar spondylolisthesis
10 0 2 7.7E-02 0 0
CUI: C0936016
Disease: Testicular Feminization
Testicular Feminization
24 0 3 7.7E-02 0 0
CUI: C1704328
Disease: Osteoblastic Osteosarcoma
Osteoblastic Osteosarcoma
10 0 2 7.7E-02 0 0
CUI: C0039093
Disease: Congenital abnormal Synostosis
Congenital abnormal Synostosis
25 0 3 7.5E-02 0 0