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: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
40 0 1 4.0E-03 0 0
CUI: C0029489
Disease: Other alopecia
Other alopecia
39 0 1 4.0E-03 0 0
CUI: C0162311
Disease: Androgenetic Alopecia
Androgenetic Alopecia
39 0 1 4.0E-03 0 0
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3
39 0 1 4.0E-03 0 0
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2
39 0 1 4.0E-03 0 0
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1
39 0 1 4.0E-03 0 0
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern
39 0 1 4.0E-03 0 0
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic
36 0 1 4.0E-03 0 0
CUI: C0272178
Disease: Drug-induced neutropenia
Drug-induced neutropenia
34 0 1 4.1E-03 0 0
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
32 0 1 4.1E-03 0 0
Malignant melanoma of skin of upper limb
32 0 1 4.1E-03 0 0
Malignant melanoma of skin of lower limb
32 0 1 4.1E-03 0 0
CUI: C0523677
Disease: Glycine measurement
Glycine measurement
32 68 1 4.1E-03 1 2.5E-03
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
30 0 1 4.1E-03 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria
29 59 1 4.1E-03 1 2.5E-03
CUI: C0017638
Disease: Glioma
Glioma
29 0 1 4.1E-03 0 0
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
28 0 1 4.2E-03 0 0
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris
28 0 1 4.2E-03 0 0
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
27 0 1 4.2E-03 0 0
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder
26 0 1 4.2E-03 0 0
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement
26 0 1 4.2E-03 0 0
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
26 0 1 4.2E-03 0 0
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1
26 0 1 4.2E-03 0 0
Amyotrophic Lateral Sclerosis, Sporadic
26 0 1 4.2E-03 0 0
Autosomal dominant compelling helio ophthalmic outburst syndrome
26 0 1 4.2E-03 0 0