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: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
285 44 1 3.5E-03 2 3.3E-02
CUI: C0016506
Disease: Foot Deformities
Foot Deformities
66 5 1 1.4E-02 2 9.1E-02
CUI: C0018099
Disease: Gout
Gout
205 2354 1 4.8E-03 2 8.4E-04
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
2322 1085 1 4.3E-04 2 1.8E-03
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria
127 17 2 1.6E-02 2 5.9E-02
CUI: C0311394
Disease: Difficulty walking
Difficulty walking
224 30 2 8.8E-03 2 4.3E-02
Central nervous system demyelination
52 3 1 1.8E-02 2 1.0E-01
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia
172 17 1 5.7E-03 2 5.9E-02
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy
93 21 1 1.0E-02 2 5.3E-02
CUI: C1836150
Disease: Gait imbalance
Gait imbalance
57 24 1 1.7E-02 2 4.9E-02
Impaired vibration sensation in the lower limbs
39 4 1 2.4E-02 2 9.5E-02
CUI: C4025609
Disease: EMG: axonal abnormality
EMG: axonal abnormality
6 4 1 0.11 2 9.5E-02
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy
271 13 1 3.6E-03 2 6.7E-02
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis
282 0 1 3.5E-03 0 0
CUI: C0002871
Disease: Anemia
Anemia
847 0 1 1.2E-03 0 0
CUI: C0002893
Disease: Refractory anemias
Refractory anemias
340 0 1 2.9E-03 0 0
Refractory anaemia with excess blasts
49 0 1 1.9E-02 0 0
CUI: C0003578
Disease: Apnea
Apnea
262 0 1 3.8E-03 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 0 2 2.3E-03 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 0 1 1.7E-03 0 0
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
6941 0 1 1.4E-04 0 0
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
8621 0 1 1.2E-04 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
441 0 1 2.3E-03 0 0
CUI: C0007933
Disease: Meibomian Cyst
Meibomian Cyst
3 0 1 0.17 0 0
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
757 0 1 1.3E-03 0 0