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: C0151772
Disease: Manic psychosis
Manic psychosis
1 0 1 0.25 0 0
CUI: C1262106
Disease: Neuromuscular toxicity
Neuromuscular toxicity
1 0 1 0.25 0 0
CUI: C3541908
Disease: Sperm Motility Measurement
Sperm Motility Measurement
1 0 1 0.25 0 0
CUI: C3715155
Disease: AMYOTROPHIC LATERAL SCLEROSIS 19
AMYOTROPHIC LATERAL SCLEROSIS 19
1 0 1 0.25 0 0
CUI: C4525499
Disease: Quail Fibrosarcoma
Quail Fibrosarcoma
1 0 1 0.25 0 0
Metastatic Oral Cavity Squamous Cell Carcinoma
1 0 1 0.25 0 0
CUI: C0154742
Disease: Other lesions of median nerve
Other lesions of median nerve
8 0 2 0.20 0 0
CUI: C3495887
Disease: ARIA-H
ARIA-H
2 0 1 0.20 0 0
Invasive Mucinous Lung Adenocarcinoma
3 0 1 0.17 0 0
CUI: C2825910
Disease: Stem Cell Factor Measurement
Stem Cell Factor Measurement
4 0 1 0.14 0 0
CUI: C0302826
Disease: Expressed Emotion
Expressed Emotion
6 0 1 0.11 0 0
CUI: C0428419
Disease: Triiodothyronine measurement
Triiodothyronine measurement
6 0 1 0.11 0 0
CUI: C2007076
Disease: Liver Carcinosarcoma
Liver Carcinosarcoma
7 0 1 1.0E-01 0 0
CUI: C3489398
Disease: Neuroepithelioma, Peripheral
Neuroepithelioma, Peripheral
7 0 1 1.0E-01 0 0
CUI: C0270855
Disease: Early myoclonic encephalopathy
Early myoclonic encephalopathy
10 0 1 7.7E-02 0 0
Congenital hypomyelinating neuropathy
11 0 1 7.1E-02 0 0
Left ventricular outflow tract obstruction
13 0 1 6.2E-02 0 0
CUI: C0876994
Disease: Cardiotoxicity
Cardiotoxicity
13 0 1 6.2E-02 0 0
CUI: C1135194
Disease: Chronic systolic heart failure
Chronic systolic heart failure
13 0 1 6.2E-02 0 0
CUI: C0233762
Disease: Hallucinations, Auditory
Hallucinations, Auditory
14 0 1 5.9E-02 0 0
CUI: C1257840
Disease: Aganglionosis, Rectosigmoid Colon
Aganglionosis, Rectosigmoid Colon
15 0 1 5.6E-02 0 0
CUI: C2112532
Disease: Postmenopausal endometrium
Postmenopausal endometrium
15 0 1 5.6E-02 0 0
CUI: C1321884
Disease: Atresia of vagina
Atresia of vagina
16 0 1 5.3E-02 0 0
CUI: C2936380
Disease: Neointima
Neointima
40 0 2 4.8E-02 0 0
CUI: C3661523
Disease: Congenital Intestinal Aganglionosis
Congenital Intestinal Aganglionosis
18 0 1 4.8E-02 0 0