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: C1839364
Disease: Progressive visual loss
Progressive visual loss
77 11 5 1.9E-02 2 5.6E-02
CUI: C1849097
Disease: Loss of ability to walk
Loss of ability to walk
37 11 7 3.2E-02 2 5.6E-02
Spastic paraplegia 11, autosomal recessive
9 134 2 1.0E-02 2 1.3E-02
CUI: C2677180
Disease: Congenital microcephaly
Congenital microcephaly
51 29 3 1.3E-02 2 3.7E-02
CUI: C3278204
Disease: Dysmyelinating leukodystrophy
Dysmyelinating leukodystrophy
4 2 4 2.1E-02 2 7.4E-02
CUI: C4025609
Disease: EMG: axonal abnormality
EMG: axonal abnormality
6 4 2 1.0E-02 2 6.9E-02
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X
1 8 1 5.3E-03 2 6.1E-02
CUI: C0002994
Disease: Angioedema
Angioedema
18 8 1 4.8E-03 1 2.9E-02
CUI: C0003635
Disease: Apraxias
Apraxias
71 9 5 2.0E-02 1 2.9E-02
CUI: C0003864
Disease: Arthritis
Arthritis
1072 69 26 2.1E-02 1 1.1E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
2723 2387 41 1.4E-02 1 4.1E-04
CUI: C0009676
Disease: Confusion
Confusion
75 5 5 1.9E-02 1 3.2E-02
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
1719 297 39 2.1E-02 1 3.1E-03
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 54 71 0.12 1 1.3E-02
CUI: C0013421
Disease: Dystonia
Dystonia
453 97 75 0.13 1 8.1E-03
CUI: C0015672
Disease: Fatigue
Fatigue
760 67 12 1.3E-02 1 1.1E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
2322 1085 52 2.1E-02 1 9.0E-04
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
613 283 19 2.4E-02 1 3.2E-03
CUI: C0023522
Disease: Leukodystrophy, Metachromatic
Leukodystrophy, Metachromatic
27 158 4 1.9E-02 1 5.4E-03
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
580 48 79 0.11 1 1.4E-02
CUI: C0027746
Disease: Nerve Degeneration
Nerve Degeneration
165 17 9 2.6E-02 1 2.3E-02
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma
344 186 8 1.5E-02 1 4.7E-03
CUI: C0037315
Disease: Sleep Apnea Syndromes
Sleep Apnea Syndromes
148 18 5 1.5E-02 1 2.3E-02
CUI: C0085632
Disease: Apathy
Apathy
83 9 3 1.1E-02 1 2.9E-02
CUI: C0162309
Disease: Adrenoleukodystrophy
Adrenoleukodystrophy
294 116 17 3.6E-02 1 7.0E-03