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: C0002418
Disease: Amblyopia
Amblyopia
85 29 1 1.1E-02 1 2.6E-02
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis
198 0 1 5.0E-03 0 0
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary
35 0 1 2.6E-02 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 1 5.2E-04 0 0
CUI: C0008489
Disease: Chorea
Chorea
168 0 2 1.2E-02 0 0
CUI: C0009024
Disease: Clonus
Clonus
60 0 1 1.6E-02 0 0
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
389 0 3 7.7E-03 0 0
Diabetes Mellitus, Non-Insulin-Dependent
3134 0 1 3.2E-04 0 0
CUI: C0013384
Disease: Dyskinetic syndrome
Dyskinetic syndrome
316 42 1 3.1E-03 1 1.9E-02
CUI: C0013421
Disease: Dystonia
Dystonia
453 0 3 6.6E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
272 0 1 3.6E-03 0 0
CUI: C0017639
Disease: Gliosis
Gliosis
102 0 1 9.5E-03 0 0
CUI: C0018975
Disease: Hemeralopia
Hemeralopia
12 0 3 0.23 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
208 0 1 4.7E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation
160 0 3 1.9E-02 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
190 0 1 5.2E-03 0 0
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial
142 0 3 2.1E-02 0 0
CUI: C0025958
Disease: Microcephaly
Microcephaly
1064 0 3 2.8E-03 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism
586 0 1 1.7E-03 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
362 0 3 8.3E-03 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
197 21 1 5.0E-03 1 3.2E-02
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
580 0 1 1.7E-03 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus
265 0 1 3.7E-03 0 0
CUI: C0027651
Disease: Neoplasms
Neoplasms
10161 0 1 9.8E-05 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex
218 0 1 4.5E-03 0 0