Source: ALL
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: C0033822
Disease: Pseudomyxoma Peritonei
Pseudomyxoma Peritonei 		0 3 0 0 3 1.00
CUI: C0206656
Disease: Embryonal Rhabdomyosarcoma
Embryonal Rhabdomyosarcoma 		0 8 0 0 2 0.22
CUI: C0242621
Disease: Isochromosomes
Isochromosomes 		0 2 0 0 2 0.67
CUI: C0279612
Disease: Childhood Embryonal Rhabdomyosarcoma
Childhood Embryonal Rhabdomyosarcoma 		0 7 0 0 2 0.25
CUI: C0346976
Disease: Secondary malignant neoplasm of pancreas
Secondary malignant neoplasm of pancreas 		0 4 0 0 2 0.40
CUI: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant 		0 2 0 0 2 0.67
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		0 2 0 0 2 0.67
CUI: C0456889
Disease: Enteropathy-Associated T-Cell Lymphoma
Enteropathy-Associated T-Cell Lymphoma 		0 3 0 0 2 0.50
CUI: C0497550
Disease: Benign neurologic neoplasms
Benign neurologic neoplasms 		0 2 0 0 2 0.67
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor 		0 93 0 0 2 2.1E-02
CUI: C1845055
Disease: ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED
ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED 		0 32 0 0 2 6.1E-02
CUI: C2930967
Disease: Gastro-enteropancreatic neuroendocrine tumor
Gastro-enteropancreatic neuroendocrine tumor 		0 4 0 0 3 0.75
CUI: C2986658
Disease: Diffuse Intrinsic Pontine Glioma
Diffuse Intrinsic Pontine Glioma 		0 9 0 0 2 0.20
CUI: C3272525
Disease: Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma
Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma 		0 2 0 0 2 0.67
CUI: C4721452
Disease: Intestinal T-Cell Lymphoma
Intestinal T-Cell Lymphoma 		0 3 0 0 2 0.50
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 1 9.1E-04 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 4.0E-03 0 0
CUI: C0000833
Disease: Abscess
Abscess 		96 0 1 1.0E-02 0 0
CUI: C0000846
Disease: Agenesis
Agenesis 		161 0 1 6.2E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 8.3E-02 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		243 0 1 4.1E-03 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly 		138 25 1 7.2E-03 2 7.7E-02
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		435 0 1 2.3E-03 0 0
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		130 0 1 7.6E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 4 1 1.0E-01 2 0.40