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: C3554105
Disease: PERRAULT SYNDROME 2
PERRAULT SYNDROME 2 		2 0 1 0.50 0 0
CUI: C3809105
Disease: PERRAULT SYNDROME 4
PERRAULT SYNDROME 4 		2 0 1 0.50 0 0
CUI: C4551721
Disease: PERRAULT SYNDROME 1
PERRAULT SYNDROME 1 		2 0 1 0.50 0 0
CUI: C1838180
Disease: CODAS syndrome
CODAS syndrome 		4 0 1 0.25 0 0
CUI: C1401084
Disease: Ovarian Insufficiency
Ovarian Insufficiency 		9 0 1 0.11 0 0
CUI: C0685838
Disease: Gonadal dysgenesis XX type deafness
Gonadal dysgenesis XX type deafness 		14 0 1 7.1E-02 0 0
CUI: C3532239
Disease: Mitochondrial cardiomyopathy
Mitochondrial cardiomyopathy 		23 0 1 4.3E-02 0 0
CUI: C0271829
Disease: Pendred's syndrome
Pendred's syndrome 		35 0 1 2.9E-02 0 0
CUI: C0747102
Disease: Ovarian failure
Ovarian failure 		39 0 1 2.6E-02 0 0
CUI: C0266399
Disease: Infantile uterus
Infantile uterus 		43 0 1 2.3E-02 0 0
CUI: C1285498
Disease: Vegetation
Vegetation 		67 0 1 1.5E-02 0 0
CUI: C1865866
Disease: Congenital sensorineural hearing loss
Congenital sensorineural hearing loss 		68 0 1 1.5E-02 0 0
CUI: C0948896
Disease: Primary hypogonadism
Primary hypogonadism 		80 0 1 1.3E-02 0 0
CUI: C0232939
Disease: Primary physiologic amenorrhea
Primary physiologic amenorrhea 		129 0 1 7.8E-03 0 0
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases 		284 0 1 3.5E-03 0 0
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		1125 0 1 8.9E-04 0 0