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: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly
45 0 1 8.1E-04 0 0
Influenza due to Influenza A virus subtype H1N1
44 0 1 8.1E-04 0 0
CUI: C1271100
Disease: Lower limb spasticity
Lower limb spasticity
43 0 1 8.1E-04 0 0
CUI: C0426818
Disease: Thin rib
Thin rib
42 0 1 8.1E-04 0 0
CUI: C0231921
Disease: Pulmonary function
Pulmonary function
41 259 1 8.1E-04 1 2.0E-03
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy
41 0 1 8.1E-04 0 0
Decreased activity of mitochondrial complex I
41 0 1 8.1E-04 0 0
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding)
41 259 1 8.1E-04 1 2.0E-03
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination
40 220 1 8.1E-04 1 2.2E-03
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
40 0 1 8.1E-04 0 0
Shortening of all distal phalanges of the fingers
40 0 1 8.1E-04 0 0
CUI: C0029489
Disease: Other alopecia
Other alopecia
39 0 1 8.1E-04 0 0
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness
39 0 1 8.1E-04 0 0
CUI: C0431350
Disease: Primary microcephaly
Primary microcephaly
39 0 1 8.1E-04 0 0
CUI: C1844548
Disease: Hypoplastic finger
Hypoplastic finger
39 0 1 8.1E-04 0 0
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3
39 0 1 8.1E-04 0 0
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2
39 0 1 8.1E-04 0 0
CUI: C2749675
Disease: Cortical gyral simplification
Cortical gyral simplification
39 0 1 8.1E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome
39 0 1 8.1E-04 0 0
Abnormal mitochondria in muscle tissue
39 0 1 8.1E-04 0 0
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1
39 0 1 8.1E-04 0 0
CUI: C0078917
Disease: Albinism, Ocular
Albinism, Ocular
37 0 1 8.2E-04 0 0
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder
37 0 1 8.2E-04 0 0
CUI: C0239594
Disease: Short finger
Short finger
37 0 1 8.2E-04 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly
37 0 1 8.2E-04 0 0