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: C0153691
Disease: Secondary malignant neoplasm of adrenal gland
Secondary malignant neoplasm of adrenal gland 		1 0 1 1.6E-02 0 0
CUI: C0155504
Disease: Serous labyrinthitis
Serous labyrinthitis 		1 0 1 1.6E-02 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 0 1 1.6E-02 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 0 1 1.6E-02 0 0
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle 		1 0 1 1.6E-02 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 1.6E-02 0 0
CUI: C0235267
Disease: Redness of eye
Redness of eye 		1 0 1 1.6E-02 0 0
CUI: C0238197
Disease: Leiomyoma of small intestine
Leiomyoma of small intestine 		1 0 1 1.6E-02 0 0
CUI: C0238517
Disease: Vaginal clear cell adenocarcinoma
Vaginal clear cell adenocarcinoma 		1 0 1 1.6E-02 0 0
CUI: C0238518
Disease: Squamous cell carcinoma of vagina
Squamous cell carcinoma of vagina 		1 0 1 1.6E-02 0 0
CUI: C0238525
Disease: Sarcoma of vulva
Sarcoma of vulva 		1 0 1 1.6E-02 0 0
CUI: C0240995
Disease: Increased serum androstenedione
Increased serum androstenedione 		1 0 1 1.6E-02 0 0
CUI: C0263442
Disease: Acne Conglobata
Acne Conglobata 		1 0 1 1.6E-02 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome 		1 0 1 1.6E-02 0 0
CUI: C0265593
Disease: Brachymetacarpia
Brachymetacarpia 		1 0 1 1.6E-02 0 0
CUI: C0265978
Disease: Collagen nevus of skin
Collagen nevus of skin 		1 0 1 1.6E-02 0 0
CUI: C0266284
Disease: Lingual Thyroid
Lingual Thyroid 		1 0 1 1.6E-02 0 0
CUI: C0267095
Disease: Leukoplakia of esophagus
Leukoplakia of esophagus 		1 0 1 1.6E-02 0 0
CUI: C0267158
Disease: Reflux gastritis
Reflux gastritis 		1 0 1 1.6E-02 0 0
CUI: C0268039
Disease: Ketoacidosis due to acute alcohol intoxication
Ketoacidosis due to acute alcohol intoxication 		1 0 1 1.6E-02 0 0
CUI: C0268373
Disease: Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
Congenital junctional epidermolysis bullosa-pyloric atresia syndrome 		1 0 1 1.6E-02 0 0
CUI: C0268500
Disease: Yellow mutant oculocutaneous albinism
Yellow mutant oculocutaneous albinism 		1 0 1 1.6E-02 0 0
CUI: C0269852
Disease: Vasa Previa
Vasa Previa 		1 0 1 1.6E-02 0 0
CUI: C0270075
Disease: Perinatal disorder
Perinatal disorder 		1 0 1 1.6E-02 0 0
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 0 1 1.6E-02 0 0