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: C1370419
Disease: Ovarian Granulosa Cell Tumor
Ovarian Granulosa Cell Tumor 		23 0 3 6.1E-02 0 0
CUI: C0032796
Disease: Postpartum Amenorrhea
Postpartum Amenorrhea 		6 0 2 6.1E-02 0 0
CUI: C0206711
Disease: Pilomatrixoma
Pilomatrixoma 		24 0 3 6.0E-02 0 0
CUI: C0936016
Disease: Testicular Feminization
Testicular Feminization 		24 0 3 6.0E-02 0 0
CUI: C0023601
Disease: Leydig Cell Tumor
Leydig Cell Tumor 		42 0 4 6.0E-02 0 0
CUI: C0042995
Disease: Vulvar Neoplasms
Vulvar Neoplasms 		7 0 2 5.9E-02 0 0
CUI: C0271287
Disease: Schnyder crystalline corneal dystrophy
Schnyder crystalline corneal dystrophy 		7 0 2 5.9E-02 0 0
CUI: C0334036
Disease: Apocrine metaplasia
Apocrine metaplasia 		7 0 2 5.9E-02 0 0
CUI: C1112338
Disease: Apoptotic DNA damage
Apoptotic DNA damage 		7 0 2 5.9E-02 0 0
CUI: C1370723
Disease: Stromal sarcoma
Stromal sarcoma 		7 0 2 5.9E-02 0 0
CUI: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic 		26 0 3 5.8E-02 0 0
CUI: C0025319
Disease: Menopausal syndrome
Menopausal syndrome 		8 0 2 5.7E-02 0 0
CUI: C0349464
Disease: Wernicke-Korsakoff Syndrome
Wernicke-Korsakoff Syndrome 		8 0 2 5.7E-02 0 0
CUI: C1412014
Disease: Infiltrating duct carcinoma
Infiltrating duct carcinoma 		8 0 2 5.7E-02 0 0
CUI: C3897045
Disease: Short Stature Homeobox Deficiency
Short Stature Homeobox Deficiency 		8 0 2 5.7E-02 0 0
CUI: C0011304
Disease: Demyelination
Demyelination 		9 0 2 5.6E-02 0 0
CUI: C0262929
Disease: Myxoma of the Endocardium
Myxoma of the Endocardium 		28 0 3 5.6E-02 0 0
CUI: C0280299
Disease: Squamous cell carcinoma of buccal mucosa
Squamous cell carcinoma of buccal mucosa 		9 0 2 5.6E-02 0 0
CUI: C0457506
Disease: Reactive thrombocytosis
Reactive thrombocytosis 		9 0 2 5.6E-02 0 0
CUI: C0555232
Disease: pseudohermaphrodite (non-specific)
pseudohermaphrodite (non-specific) 		9 0 2 5.6E-02 0 0
CUI: C1848411
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E 		9 0 2 5.6E-02 0 0
CUI: C2350037
Disease: Clinically Isolated Syndrome, CNS Demyelinating
Clinically Isolated Syndrome, CNS Demyelinating 		9 0 2 5.6E-02 0 0
CUI: C0151900
Disease: Serum iron raised
Serum iron raised 		10 0 2 5.4E-02 0 0
CUI: C0158447
Disease: Idiopathic osteoporosis
Idiopathic osteoporosis 		10 0 2 5.4E-02 0 0
CUI: C0238394
Disease: Female Pseudohermaphroditism
Female Pseudohermaphroditism 		10 0 2 5.4E-02 0 0