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: C0406438
Disease: Pterygium of nail
Pterygium of nail
4 0 4 0.15 0 0
CUI: C1840283
Disease: ICHTHYOSIS--CHEEK--EYEBROW SYNDROME
ICHTHYOSIS--CHEEK--EYEBROW SYNDROME
5 0 4 0.15 0 0
CUI: C4524073
Disease: Low anterior resection syndrome
Low anterior resection syndrome
4 0 3 0.11 0 0
CUI: C3160821
Disease: Viral uveitis
Viral uveitis
5 0 3 0.11 0 0
CUI: C1846142
Disease: HOYERAAL-HREIDARSSON SYNDROME
HOYERAAL-HREIDARSSON SYNDROME
16 0 4 0.11 0 0
CUI: C0014866
Disease: Esophageal Stenosis
Esophageal Stenosis
17 0 4 0.10 0 0
CUI: C0239804
Disease: White hair
White hair
18 0 4 1.0E-01 0 0
CUI: C1855204
Disease: Cellular immunodeficiency
Cellular immunodeficiency
30 0 5 9.8E-02 0 0
CUI: C4020958
Disease: Rough bone trabeculation
Rough bone trabeculation
19 0 4 9.8E-02 0 0
CUI: C3279575
Disease: Reticulated skin pigmentation
Reticulated skin pigmentation
8 0 3 9.7E-02 0 0
CUI: C3814530
Disease: Skin Vesicle
Skin Vesicle
20 0 4 9.5E-02 0 0
CUI: C0432330
Disease: Erythrokeratoderma
Erythrokeratoderma
10 0 3 9.1E-02 0 0
CUI: C1856749
Disease: Aplastic/hypoplastic toenail
Aplastic/hypoplastic toenail
23 0 4 8.9E-02 0 0
CUI: C4025838
Disease: Abnormality of the pharynx
Abnormality of the pharynx
23 0 4 8.9E-02 0 0
CUI: C1281931
Disease: Obstruction of nasolacrimal duct
Obstruction of nasolacrimal duct
12 0 3 8.6E-02 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 4 7.8E-02 0 0
CUI: C4024737
Disease: Aplasia/Hypoplasia of the skin
Aplasia/Hypoplasia of the skin
29 0 4 7.8E-02 0 0
Abnormality of female internal genitalia
31 0 4 7.5E-02 0 0
Dyskeratosis Congenita, Autosomal Recessive
3 0 2 7.4E-02 0 0
Punctate opacification of the cornea
3 0 2 7.4E-02 0 0
CUI: C0025221
Disease: Meleda Disease
Meleda Disease
18 0 3 7.3E-02 0 0
CUI: C0263498
Disease: Premature canities
Premature canities
33 4 4 7.3E-02 1 0.20
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT
4 0 2 7.1E-02 0 0
CUI: C4551650
Disease: Esophageal Stricture
Esophageal Stricture
20 0 3 7.0E-02 0 0
CUI: C0409983
Disease: Secondary antiphospholipid syndrome
Secondary antiphospholipid syndrome
6 0 2 6.7E-02 0 0