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: C0014866
Disease: Esophageal Stenosis
Esophageal Stenosis
17 0 11 0.24 0 0
CUI: C0239804
Disease: White hair
White hair
18 0 11 0.23 0 0
CUI: C4020958
Disease: Rough bone trabeculation
Rough bone trabeculation
19 0 11 0.23 0 0
CUI: C3814530
Disease: Skin Vesicle
Skin Vesicle
20 0 11 0.22 0 0
CUI: C1856749
Disease: Aplastic/hypoplastic toenail
Aplastic/hypoplastic toenail
23 0 11 0.21 0 0
CUI: C4025838
Disease: Abnormality of the pharynx
Abnormality of the pharynx
23 0 11 0.21 0 0
CUI: C4024737
Disease: Aplasia/Hypoplasia of the skin
Aplasia/Hypoplasia of the skin
29 0 12 0.21 0 0
CUI: C1846142
Disease: HOYERAAL-HREIDARSSON SYNDROME
HOYERAAL-HREIDARSSON SYNDROME
16 0 9 0.19 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 11 0.19 0 0
CUI: C1855204
Disease: Cellular immunodeficiency
Cellular immunodeficiency
30 0 11 0.19 0 0
Abnormality of female internal genitalia
31 0 11 0.18 0 0
CUI: C0263498
Disease: Premature canities
Premature canities
33 0 11 0.18 0 0
CUI: C0041974
Disease: Urethral Stenosis
Urethral Stenosis
41 0 12 0.17 0 0
CUI: C2675111
Disease: Abnormal eyelash morphology
Abnormal eyelash morphology
39 0 11 0.16 0 0
CUI: C0085660
Disease: Aseptic necrosis
Aseptic necrosis
41 0 11 0.16 0 0
CUI: C3887513
Disease: Avascular necrosis
Avascular necrosis
41 0 11 0.16 0 0
CUI: C4553018
Disease: Avascular Necrosis, CTCAE
Avascular Necrosis, CTCAE
41 0 11 0.16 0 0
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation
59 0 13 0.15 0 0
CUI: C0005741
Disease: Blepharitis
Blepharitis
55 0 12 0.14 0 0
CUI: C1837770
Disease: Sparse hair
Sparse hair
112 0 19 0.14 0 0
CUI: C1842774
Disease: Hypermelanotic macule
Hypermelanotic macule
59 0 12 0.14 0 0
CUI: C4021787
Disease: Abnormal diaphysis morphology
Abnormal diaphysis morphology
11 0 6 0.13 0 0
CUI: C4022018
Disease: Telangiectasia of the skin
Telangiectasia of the skin
56 0 11 0.13 0 0
CUI: C0265965
Disease: Dyskeratosis Congenita
Dyskeratosis Congenita
58 0 11 0.13 0 0
CUI: C4727832
Disease: Telomere Syndrome
Telomere Syndrome
5 0 5 0.12 0 0