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: C0018552
Disease: Hamartoma
Hamartoma 		4 0 1 3.3E-02 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		37 0 1 1.6E-02 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		31 0 1 1.8E-02 0 0
CUI: C0018932
Disease: Hematochezia
Hematochezia 		2 0 1 3.6E-02 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		25 0 1 2.0E-02 0 0
CUI: C0020437
Disease: Hypercalcemia
Hypercalcemia 		4 0 1 3.3E-02 0 0
CUI: C0020502
Disease: Hyperparathyroidism
Hyperparathyroidism 		1 0 1 3.7E-02 0 0
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia 		2 0 1 3.6E-02 0 0
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		25 0 2 4.0E-02 0 0
CUI: C0022821
Disease: Kyphosis deformity of spine
Kyphosis deformity of spine 		9 0 1 2.9E-02 0 0
CUI: C0023418
Disease: leukemia
leukemia 		2 0 1 3.6E-02 0 0
CUI: C0023462
Disease: Acute Megakaryocytic Leukemias
Acute Megakaryocytic Leukemias 		4 0 2 6.9E-02 0 0
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic 		5 0 1 3.2E-02 0 0
CUI: C0023798
Disease: Lipoma
Lipoma 		5 0 1 3.2E-02 0 0
CUI: C0023882
Disease: Little's Disease
Little's Disease 		6 0 1 3.1E-02 0 0
CUI: C0024221
Disease: Lymphangioma
Lymphangioma 		1 0 1 3.7E-02 0 0
CUI: C0024421
Disease: Macroglossia
Macroglossia 		2 0 1 3.6E-02 0 0
CUI: C0024433
Disease: Macrostomia
Macrostomia 		10 0 1 2.8E-02 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		162 0 5 2.7E-02 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		28 0 1 1.9E-02 0 0
CUI: C0027022
Disease: Myeloproliferative disease
Myeloproliferative disease 		5 0 1 3.2E-02 0 0
CUI: C0027092
Disease: Myopia
Myopia 		45 0 1 1.4E-02 0 0
CUI: C0027960
Disease: Nevus
Nevus 		4 0 1 3.3E-02 0 0
CUI: C0028754
Disease: Obesity
Obesity 		24 0 1 2.0E-02 0 0
CUI: C0030521
Disease: Parathyroid Neoplasms
Parathyroid Neoplasms 		1 0 1 3.7E-02 0 0