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: C1846142
Disease: HOYERAAL-HREIDARSSON SYNDROME
HOYERAAL-HREIDARSSON SYNDROME
16 0 1 5.9E-02 0 0
CUI: C0014866
Disease: Esophageal Stenosis
Esophageal Stenosis
17 0 1 5.6E-02 0 0
HODGKIN'S AND NON-HODGKIN'S LYMPHOMA
17 0 1 5.6E-02 0 0
CUI: C0456861
Disease: Low grade B-cell lymphoma
Low grade B-cell lymphoma
17 0 1 5.6E-02 0 0
CUI: C1148551
Disease: X-Linked Dyskeratosis Congenita
X-Linked Dyskeratosis Congenita
17 0 1 5.6E-02 0 0
CUI: C0239804
Disease: White hair
White hair
18 0 1 5.3E-02 0 0
CUI: C4020958
Disease: Rough bone trabeculation
Rough bone trabeculation
19 0 1 5.0E-02 0 0
CUI: C1334634
Disease: Mature B-Cell Non-Hodgkin Lymphoma
Mature B-Cell Non-Hodgkin Lymphoma
20 0 1 4.8E-02 0 0
CUI: C3814530
Disease: Skin Vesicle
Skin Vesicle
20 0 1 4.8E-02 0 0
CUI: C4721508
Disease: Hamman-Rich Disease
Hamman-Rich Disease
20 0 1 4.8E-02 0 0
CUI: C0034088
Disease: Pulmonary Valve Insufficiency
Pulmonary Valve Insufficiency
22 0 1 4.3E-02 0 0
Post-transplant lymphoproliferative disorder
22 0 1 4.3E-02 0 0
CUI: C2826321
Disease: Refractory Thrombocytopenia
Refractory Thrombocytopenia
22 0 1 4.3E-02 0 0
CUI: C0034642
Disease: Rales
Rales
23 0 1 4.2E-02 0 0
CUI: C1856749
Disease: Aplastic/hypoplastic toenail
Aplastic/hypoplastic toenail
23 0 1 4.2E-02 0 0
CUI: C4025838
Disease: Abnormality of the pharynx
Abnormality of the pharynx
23 0 1 4.2E-02 0 0
CUI: C4049273
Disease: Systemic immune activation
Systemic immune activation
23 0 1 4.2E-02 0 0
Familial Idiopathic Pulmonary Fibrosis
23 0 1 4.2E-02 0 0
CUI: C0855146
Disease: B Lymphoblastic Lymphoma
B Lymphoblastic Lymphoma
25 0 1 3.8E-02 0 0
CUI: C4024890
Disease: Excessive wrinkled skin
Excessive wrinkled skin
25 0 1 3.8E-02 0 0
CUI: C1334170
Disease: Indolent Non-Hodgkin Lymphoma
Indolent Non-Hodgkin Lymphoma
27 0 1 3.6E-02 0 0
CUI: C0079746
Disease: Immunoblastic Large-Cell Lymphoma
Immunoblastic Large-Cell Lymphoma
28 0 1 3.4E-02 0 0
CUI: C0265965
Disease: Dyskeratosis Congenita
Dyskeratosis Congenita
58 146 2 3.4E-02 1 6.8E-03
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 1 3.3E-02 0 0
CUI: C4024737
Disease: Aplasia/Hypoplasia of the skin
Aplasia/Hypoplasia of the skin
29 0 1 3.3E-02 0 0