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: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
58 5 1 1.7E-02 1 5.9E-02
CUI: C0035300
Disease: Abnormal retinal morphology
Abnormal retinal morphology
13 0 1 7.7E-02 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential
55 0 1 1.8E-02 0 0
CUI: C4024172
Disease: Abnormality of hair pigmentation
Abnormality of hair pigmentation
5 2 1 0.20 1 7.1E-02
Abnormality of metabolism/homeostasis
171 5 1 5.8E-03 2 0.12
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 4.7E-03 0 0
CUI: C4316870
Disease: Abnormality of the eye
Abnormality of the eye
56 0 1 1.8E-02 0 0
CUI: C0029131
Disease: Abnormality of the optic nerve
Abnormality of the optic nerve
18 0 1 5.6E-02 0 0
CUI: C2673954
Disease: Absent skin pigmentation
Absent skin pigmentation
1 0 1 1.00 0 0
CUI: C0262977
Disease: Achromia of skin
Achromia of skin
7 0 1 0.14 0 0
CUI: C0022602
Disease: Actinic keratosis
Actinic keratosis
136 0 1 7.4E-03 0 0
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
405 0 1 2.5E-03 0 0
CUI: C1313983
Disease: Acute contagious conjunctivitis
Acute contagious conjunctivitis
1 0 1 1.00 0 0
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
440 0 1 2.3E-03 0 0
CUI: C0022672
Disease: Acute Kidney Tubular Necrosis
Acute Kidney Tubular Necrosis
53 0 1 1.9E-02 0 0
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
639 0 1 1.6E-03 0 0
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
633 0 1 1.6E-03 0 0
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
766 0 1 1.3E-03 0 0
CUI: C0278592
Disease: Adult Angiosarcoma
Adult Angiosarcoma
101 0 1 9.9E-03 0 0
CUI: C0023493
Disease: Adult T-Cell Lymphoma/Leukemia
Adult T-Cell Lymphoma/Leukemia
540 0 1 1.9E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 27 1 2.2E-02 8 0.25
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells
9 0 1 0.11 0 0
CUI: C0078917
Disease: Albinism, Ocular
Albinism, Ocular
37 10 1 2.7E-02 3 0.15
ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder)
3 2 1 0.33 1 7.1E-02
ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder)
2 14 1 0.50 13 0.93