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: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms 		1 0 1 0.50 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma 		1 2 1 0.50 2 0.67
CUI: C0149704
Disease: Gingivostomatitis
Gingivostomatitis 		1 0 1 0.50 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 0.50 0 0
CUI: C0241518
Disease: Retraction of tympanic membrane
Retraction of tympanic membrane 		1 0 1 0.50 0 0
CUI: C0278600
Disease: Childhood Brain Stem Glioma
Childhood Brain Stem Glioma 		1 0 1 0.50 0 0
CUI: C0302323
Disease: Reticulohistiocytosis
Reticulohistiocytosis 		1 2 1 0.50 2 0.67
CUI: C0342959
Disease: Sepsis-associated organ dysfunction
Sepsis-associated organ dysfunction 		1 0 1 0.50 0 0
CUI: C0349533
Disease: Lymphoma of intestine
Lymphoma of intestine 		1 2 1 0.50 2 0.67
CUI: C0521579
Disease: Congenital strabismus
Congenital strabismus 		1 0 1 0.50 0 0