Source: CLINVAR ×
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: C0011581
Disease: Depressive disorder
Depressive disorder 		7 0 1 2.7E-02 0 0
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		6 0 1 2.8E-02 0 0
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		29 0 1 1.7E-02 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		34 0 1 1.6E-02 0 0
CUI: C0013404
Disease: Dyspnea
Dyspnea 		18 0 1 2.1E-02 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		33 0 1 1.6E-02 0 0
CUI: C0015672
Disease: Fatigue
Fatigue 		18 0 1 2.1E-02 0 0
CUI: C0017097
Disease: Gardner Syndrome
Gardner Syndrome 		1 0 1 3.2E-02 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma 		6 0 1 2.8E-02 0 0
CUI: C0018552
Disease: Hamartoma
Hamartoma 		4 0 1 2.9E-02 0 0
CUI: C0018681
Disease: Headache
Headache 		19 0 1 2.0E-02 0 0
CUI: C0018799
Disease: Heart Diseases
Heart Diseases 		1 0 1 3.2E-02 0 0
CUI: C0018808
Disease: Heart murmur
Heart murmur 		11 0 1 2.4E-02 0 0
CUI: C0018916
Disease: Hemangioma
Hemangioma 		12 0 2 4.9E-02 0 0
CUI: C0018923
Disease: Hemangiosarcoma
Hemangiosarcoma 		2 0 1 3.1E-02 0 0
CUI: C0018932
Disease: Hematochezia
Hematochezia 		2 0 1 3.1E-02 0 0
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		21 0 1 2.0E-02 0 0
CUI: C0020437
Disease: Hypercalcemia
Hypercalcemia 		4 0 1 2.9E-02 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia 		16 0 1 2.2E-02 0 0
CUI: C0020502
Disease: Hyperparathyroidism
Hyperparathyroidism 		1 0 1 3.2E-02 0 0
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		25 0 1 1.8E-02 0 0
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia 		2 0 1 3.1E-02 0 0
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		25 0 3 5.7E-02 0 0
CUI: C0021846
Disease: Intestinal Polyps
Intestinal Polyps 		1 0 1 3.2E-02 0 0
CUI: C0022821
Disease: Kyphosis deformity of spine
Kyphosis deformity of spine 		9 0 1 2.6E-02 0 0