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: C4477094
Disease: Abnormal visual fixation
Abnormal visual fixation 		1 0 1 9.1E-02 0 0
CUI: C4509836
Disease: Familial acute necrotizing encephalopathy
Familial acute necrotizing encephalopathy 		1 0 1 9.1E-02 0 0
CUI: C4707290
Disease: BAP1 tumor predisposition syndrome
BAP1 tumor predisposition syndrome 		1 0 1 9.1E-02 0 0
CUI: C4725876
Disease: Resectable Neuroblastoma
Resectable Neuroblastoma 		1 0 1 9.1E-02 0 0
CUI: C4725878
Disease: Unresectable Neuroblastoma
Unresectable Neuroblastoma 		1 0 1 9.1E-02 0 0
CUI: C4732790
Disease: Abnormal putamen morphology
Abnormal putamen morphology 		1 0 1 9.1E-02 0 0
CUI: C0393626
Disease: Opsoclonus-Myoclonus Syndrome
Opsoclonus-Myoclonus Syndrome 		14 0 2 8.7E-02 0 0
CUI: C0018199
Disease: Granuloma, Plasma Cell
Granuloma, Plasma Cell 		2 0 1 8.3E-02 0 0
CUI: C0022078
Disease: Iris Diseases
Iris Diseases 		2 0 1 8.3E-02 0 0
CUI: C0025210
Disease: Ocular melanosis
Ocular melanosis 		2 0 1 8.3E-02 0 0
CUI: C0032541
Disease: Polyneuritis
Polyneuritis 		2 0 1 8.3E-02 0 0
CUI: C0235840
Disease: Neonatal diarrhea
Neonatal diarrhea 		2 0 1 8.3E-02 0 0
CUI: C0240564
Disease: Pain of nose
Pain of nose 		2 0 1 8.3E-02 0 0
CUI: C0268497
Disease: Brown oculocutaneous albinism
Brown oculocutaneous albinism 		2 0 1 8.3E-02 0 0
CUI: C0339619
Disease: Congenital esotropia
Congenital esotropia 		2 0 1 8.3E-02 0 0
CUI: C1333967
Disease: Inflammatory pseudotumor of liver
Inflammatory pseudotumor of liver 		2 0 1 8.3E-02 0 0
CUI: C1368275
Disease: Pigmented Basal Cell Carcinoma
Pigmented Basal Cell Carcinoma 		28 0 3 8.3E-02 0 0
CUI: C1517444
Disease: Ganglioneuroblastoma, Intermixed
Ganglioneuroblastoma, Intermixed 		2 0 1 8.3E-02 0 0
CUI: C1704237
Disease: Trichodiscoma
Trichodiscoma 		2 0 1 8.3E-02 0 0
CUI: C1832334
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D 		2 0 1 8.3E-02 0 0
CUI: C1835054
Disease: OCULOCUTANEOUS ALBINISM, TYPE II, MODIFIER OF
OCULOCUTANEOUS ALBINISM, TYPE II, MODIFIER OF 		2 0 1 8.3E-02 0 0
CUI: C1838333
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4 		2 0 1 8.3E-02 0 0
CUI: C1848435
Disease: WOOLLY HAIR, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT HYPOTRICHOSIS
WOOLLY HAIR, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT HYPOTRICHOSIS 		2 0 1 8.3E-02 0 0
CUI: C1867289
Disease: Retinal calcification
Retinal calcification 		2 0 1 8.3E-02 0 0
CUI: C1882081
Disease: Nevoid Melanoma
Nevoid Melanoma 		2 0 1 8.3E-02 0 0