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: C0027813
Disease: Neuritis
Neuritis
32 0 1 2.9E-02 0 0
CUI: C1852373
Disease: Mitochondrial encephalopathy
Mitochondrial encephalopathy
32 0 1 2.9E-02 0 0
CUI: C0742468
Disease: Central nervous system lesion
Central nervous system lesion
34 0 1 2.7E-02 0 0
CUI: C0243010
Disease: Viral Encephalitis
Viral Encephalitis
35 0 1 2.6E-02 0 0
CUI: C0030389
Disease: Parainfluenza
Parainfluenza
36 0 1 2.6E-02 0 0
CUI: C1095979
Disease: Progressive multiple sclerosis
Progressive multiple sclerosis
37 0 1 2.5E-02 0 0
CUI: C4543807
Disease: Clinical malaria
Clinical malaria
37 0 1 2.5E-02 0 0
CUI: C0025048
Disease: Meconium Aspiration Syndrome
Meconium Aspiration Syndrome
38 0 1 2.4E-02 0 0
CUI: C0221106
Disease: Alkalemia
Alkalemia
38 0 1 2.4E-02 0 0
CUI: C0276609
Disease: Acute type B viral hepatitis
Acute type B viral hepatitis
38 0 1 2.4E-02 0 0
CUI: C0280783
Disease: Juvenile Pilocytic Astrocytoma
Juvenile Pilocytic Astrocytoma
38 0 1 2.4E-02 0 0
CUI: C0272178
Disease: Drug-induced neutropenia
Drug-induced neutropenia
41 0 1 2.3E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 1 2.3E-02 0 0
CUI: C0276653
Disease: Invasive Pulmonary Aspergillosis
Invasive Pulmonary Aspergillosis
42 0 1 2.2E-02 0 0
CUI: C0751434
Disease: Classical phenylketonuria
Classical phenylketonuria
42 0 1 2.2E-02 0 0
CUI: C3179455
Disease: Niemann-Pick Disease, Type C1
Niemann-Pick Disease, Type C1
43 0 1 2.2E-02 0 0
CUI: C0242292
Disease: McCune-Albright Syndrome
McCune-Albright Syndrome
45 0 1 2.1E-02 0 0
CUI: C0023186
Disease: Learning Disorders
Learning Disorders
46 0 1 2.0E-02 0 0
CUI: C0458219
Disease: Complex Regional Pain Syndromes
Complex Regional Pain Syndromes
47 0 1 2.0E-02 0 0
CUI: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A
48 0 1 2.0E-02 0 0
malignant neoplasm of breast staging
49 0 1 1.9E-02 0 0
CUI: C2698259
Disease: Monoclonal B-Cell Lymphocytosis
Monoclonal B-Cell Lymphocytosis
49 0 1 1.9E-02 0 0
CUI: C0342208
Disease: Multinodular goiter
Multinodular goiter
51 0 1 1.9E-02 0 0
Generalized glycogen storage disease of infants
51 0 1 1.9E-02 0 0
CUI: C1855496
Disease: Contiguous gene syndrome
Contiguous gene syndrome
52 0 1 1.8E-02 0 0