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: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome
0 3 0 0 1 8.3E-02
CUI: C0242453
Disease: Prostatism
Prostatism
0 1 0 0 1 1.0E-01
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 6.2E-02
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen
0 2 0 0 2 0.20
CUI: C1290073
Disease: Acute mucositis
Acute mucositis
0 1 0 0 1 1.0E-01
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
272 0 1 2.1E-03 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
190 0 1 2.6E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 1 2.7E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia
172 0 1 2.7E-03 0 0
Child Development Disorders, Pervasive
168 0 1 2.8E-03 0 0
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders
167 0 1 2.8E-03 0 0
CUI: C1852197
Disease: MAJOR AFFECTIVE DISORDER 1
MAJOR AFFECTIVE DISORDER 1
161 0 1 2.8E-03 0 0
CUI: C1970943
Disease: MAJOR AFFECTIVE DISORDER 4
MAJOR AFFECTIVE DISORDER 4
160 0 1 2.8E-03 0 0
CUI: C1970945
Disease: MAJOR AFFECTIVE DISORDER 6
MAJOR AFFECTIVE DISORDER 6
160 0 1 2.8E-03 0 0
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
160 0 1 2.8E-03 0 0
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
149 0 1 2.9E-03 0 0
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
144 0 1 2.9E-03 0 0
CUI: C1868571
Disease: Highly arched eyebrow
Highly arched eyebrow
141 0 1 3.0E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color
130 0 1 3.1E-03 0 0
CUI: C2700438
Disease: MAJOR AFFECTIVE DISORDER 7
MAJOR AFFECTIVE DISORDER 7
127 0 1 3.1E-03 0 0
CUI: C2700439
Disease: MAJOR AFFECTIVE DISORDER 8
MAJOR AFFECTIVE DISORDER 8
126 0 1 3.1E-03 0 0
CUI: C2700440
Disease: MAJOR AFFECTIVE DISORDER 9
MAJOR AFFECTIVE DISORDER 9
126 0 1 3.1E-03 0 0
CUI: C0020649
Disease: Hypotension
Hypotension
125 0 1 3.1E-03 0 0
CUI: C0030232
Disease: Pallor
Pallor
124 0 1 3.1E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary
123 0 1 3.1E-03 0 0