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 0.33 0 0
CUI: C0040422
Disease: Tonsillar Neoplasms
Tonsillar Neoplasms
1 0 1 0.33 0 0
CUI: C0153618
Disease: Malignant tumor of renal pelvis
Malignant tumor of renal pelvis
1 0 1 0.33 0 0
CUI: C0241060
Disease: Cyst of skin
Cyst of skin
1 0 1 0.33 0 0
CUI: C0333372
Disease: Abscess cavity
Abscess cavity
1 0 1 0.33 0 0
CUI: C0333648
Disease: Abiotrophy
Abiotrophy
1 0 1 0.33 0 0
Congenital hypertrophy of retinal pigment epithelium
5 0 2 0.33 0 0
CUI: C0442774
Disease: Visual acuity, no light perception
Visual acuity, no light perception
1 0 1 0.33 0 0
CUI: C1332860
Disease: Cauda Equina Paraganglioma
Cauda Equina Paraganglioma
1 0 1 0.33 0 0
CUI: C1335749
Disease: Renal Pelvis Carcinoma
Renal Pelvis Carcinoma
1 0 1 0.33 0 0
CUI: C1519703
Disease: Turcot Syndrome Type 2
Turcot Syndrome Type 2
1 0 1 0.33 0 0
Colorectal Adenomatous Polyposis, Autosomal Recessive
1 112 1 0.33 1 8.9E-03
Paragangliomas with Sensorineural Hearing Loss
1 0 1 0.33 0 0
BRAIN TUMOR-POLYPOSIS SYNDROME 2 (disorder)
1 0 1 0.33 0 0
ADENOMATOUS POLYPOSIS COLI WITH CONGENITAL CHOLESTEATOMA
1 0 1 0.33 0 0
PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS
1 0 1 0.33 0 0
Fatal infantile mitochondrial cardiomyopathy
1 0 1 0.33 0 0
CUI: C3665800
Disease: Streptococcal endocarditis
Streptococcal endocarditis
1 0 1 0.33 0 0
FAMILIAL ADENOMATOUS POLYPOSIS 2 WITH PILOMATRICOMAS
1 1 1 0.33 1 1.00
FAMILIAL ADENOMATOUS POLYPOSIS 1, SUSCEPTIBILITY TO
1 0 1 0.33 0 0
CUI: C4021146
Disease: Hyperpigmentation of the fundus
Hyperpigmentation of the fundus
1 0 1 0.33 0 0
CUI: C4022005
Disease: Carotid paraganglioma
Carotid paraganglioma
1 0 1 0.33 0 0
CUI: C4282032
Disease: Senile hyperkeratosis
Senile hyperkeratosis
1 0 1 0.33 0 0
Abnormal B-type natriuretic peptide level
1 0 1 0.33 0 0
CUI: C4744430
Disease: Recurrent Desmoid-Type Fibromatosis
Recurrent Desmoid-Type Fibromatosis
1 0 1 0.33 0 0