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: C0034882
Disease: Rectal Diseases
Rectal Diseases 		1 0 1 0.20 0 0
CUI: C0040422
Disease: Tonsillar Neoplasms
Tonsillar Neoplasms 		1 0 1 0.20 0 0
CUI: C0153618
Disease: Malignant tumor of renal pelvis
Malignant tumor of renal pelvis 		1 0 1 0.20 0 0
CUI: C0241060
Disease: Cyst of skin
Cyst of skin 		1 0 1 0.20 0 0
CUI: C0279697
Disease: salivary gland squamous cell carcinoma
salivary gland squamous cell carcinoma 		1 0 1 0.20 0 0
CUI: C0333372
Disease: Abscess cavity
Abscess cavity 		1 0 1 0.20 0 0
CUI: C0333648
Disease: Abiotrophy
Abiotrophy 		1 0 1 0.20 0 0
CUI: C0334338
Disease: Endometrioid adenoma, borderline malignancy
Endometrioid adenoma, borderline malignancy 		1 0 1 0.20 0 0
CUI: C0334566
Disease: Ghost Cell Odontogenic Carcinoma
Ghost Cell Odontogenic Carcinoma 		1 0 1 0.20 0 0
CUI: C0406571
Disease: Superficial fibromatosis
Superficial fibromatosis 		1 0 1 0.20 0 0
CUI: C0442774
Disease: Visual acuity, no light perception
Visual acuity, no light perception 		1 0 1 0.20 0 0
CUI: C1275420
Disease: Extra-abdominal fibromatosis
Extra-abdominal fibromatosis 		1 0 1 0.20 0 0
CUI: C1333117
Disease: Colorectal Tubular Adenoma
Colorectal Tubular Adenoma 		1 0 1 0.20 0 0
CUI: C1333322
Disease: Duodenal Villous Adenoma
Duodenal Villous Adenoma 		1 0 1 0.20 0 0
CUI: C1335749
Disease: Renal Pelvis Carcinoma
Renal Pelvis Carcinoma 		1 0 1 0.20 0 0
CUI: C1519703
Disease: Turcot Syndrome Type 2
Turcot Syndrome Type 2 		1 0 1 0.20 0 0
CUI: C1704219
Disease: Dentinogenic Ghost Cell Tumor
Dentinogenic Ghost Cell Tumor 		1 0 1 0.20 0 0
CUI: C1837991
Disease: Colorectal Adenomatous Polyposis, Autosomal Recessive
Colorectal Adenomatous Polyposis, Autosomal Recessive 		1 0 1 0.20 0 0
CUI: C2673218
Disease: BRAIN TUMOR-POLYPOSIS SYNDROME 2 (disorder)
BRAIN TUMOR-POLYPOSIS SYNDROME 2 (disorder) 		1 0 1 0.20 0 0
CUI: C2673229
Disease: ADENOMATOUS POLYPOSIS COLI WITH CONGENITAL CHOLESTEATOMA
ADENOMATOUS POLYPOSIS COLI WITH CONGENITAL CHOLESTEATOMA 		1 0 1 0.20 0 0
CUI: C3266155
Disease: Functional abdominal pain syndrome
Functional abdominal pain syndrome 		1 0 1 0.20 0 0
CUI: C3554449
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 19
MENTAL RETARDATION, AUTOSOMAL DOMINANT 19 		1 0 1 0.20 0 0
CUI: C3665800
Disease: Streptococcal endocarditis
Streptococcal endocarditis 		1 0 1 0.20 0 0
CUI: C3887926
Disease: CATARACT 32, MULTIPLE TYPES
CATARACT 32, MULTIPLE TYPES 		1 0 1 0.20 0 0
CUI: C4016911
Disease: FAMILIAL ADENOMATOUS POLYPOSIS 2 WITH PILOMATRICOMAS
FAMILIAL ADENOMATOUS POLYPOSIS 2 WITH PILOMATRICOMAS 		1 0 1 0.20 0 0