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: C0220761
Disease: Dizygotic twins (disorder)
Dizygotic twins (disorder) 		1 0 1 1.0E-01 0 0
CUI: C0233200
Disease: Cullen's sign
Cullen's sign 		1 0 1 1.0E-01 0 0
CUI: C1382398
Disease: Increased capillary permeability (finding)
Increased capillary permeability (finding) 		1 0 1 1.0E-01 0 0
CUI: C1845294
Disease: Ovarian Dysgenesis 2
Ovarian Dysgenesis 2 		1 0 1 1.0E-01 0 0
CUI: C1845295
Disease: Premature Ovarian Failure 4
Premature Ovarian Failure 4 		1 0 1 1.0E-01 0 0
CUI: C2585739
Disease: Hyperreactio luteinalis
Hyperreactio luteinalis 		1 0 1 1.0E-01 0 0
CUI: C2673642
Disease: Combined Oxidative Phosphorylation Deficiency 5
Combined Oxidative Phosphorylation Deficiency 5 		1 0 1 1.0E-01 0 0
CUI: C2673646
Disease: Antenatal onset
Antenatal onset 		1 0 1 1.0E-01 0 0
CUI: C2751825
Disease: PREMATURE OVARIAN FAILURE 7 (disorder)
PREMATURE OVARIAN FAILURE 7 (disorder) 		1 0 1 1.0E-01 0 0
CUI: C2936420
Disease: 46, XX Gonadal Sex Reversal
46, XX Gonadal Sex Reversal 		1 0 1 1.0E-01 0 0
CUI: C3151406
Disease: SPERMATOGENIC FAILURE 8
SPERMATOGENIC FAILURE 8 		1 0 1 1.0E-01 0 0
CUI: C3280471
Disease: OVARIAN DYSGENESIS 3
OVARIAN DYSGENESIS 3 		1 0 1 1.0E-01 0 0
CUI: C3494162
Disease: Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous
Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous 		1 0 1 1.0E-01 0 0
CUI: C3554634
Disease: Light complexion
Light complexion 		1 0 1 1.0E-01 0 0
CUI: C3805515
Disease: Microorchidism
Microorchidism 		1 0 1 1.0E-01 0 0
CUI: C4225228
Disease: NEPHROTIC SYNDROME, TYPE 11
NEPHROTIC SYNDROME, TYPE 11 		1 0 1 1.0E-01 0 0
CUI: C4479664
Disease: ADRENAL INSUFFICIENCY, NR5A1-RELATED
ADRENAL INSUFFICIENCY, NR5A1-RELATED 		1 0 1 1.0E-01 0 0
CUI: C4748084
Disease: OVARIAN DYSGENESIS 6
OVARIAN DYSGENESIS 6 		1 0 1 1.0E-01 0 0
CUI: C4748263
Disease: OVARIAN DYSGENESIS 7
OVARIAN DYSGENESIS 7 		1 0 1 1.0E-01 0 0
CUI: C0403810
Disease: Oligosynaptic Infertility
Oligosynaptic Infertility 		2 0 1 9.1E-02 0 0
CUI: C0473311
Disease: Hemorrhagic cyst of ovary
Hemorrhagic cyst of ovary 		2 0 1 9.1E-02 0 0
CUI: C0949331
Disease: Gonadal Agenesis
Gonadal Agenesis 		2 0 1 9.1E-02 0 0
CUI: C2118097
Disease: Agonadism
Agonadism 		2 0 1 9.1E-02 0 0
CUI: C3281192
Disease: INFANTILE CEREBELLAR-RETINAL DEGENERATION
INFANTILE CEREBELLAR-RETINAL DEGENERATION 		2 0 1 9.1E-02 0 0
CUI: C3469528
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP L
FANCONI ANEMIA, COMPLEMENTATION GROUP L 		2 0 1 9.1E-02 0 0