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: C1275273
Disease: Familial Multiple Lipomatosis
Familial Multiple Lipomatosis 		3 0 1 0.12 0 0
CUI: C1609519
Disease: Myelolipoma of adrenal gland
Myelolipoma of adrenal gland 		3 0 1 0.12 0 0
CUI: C2748557
Disease: Immune dysfunction with T-cell inactivation due to calcium entry defect 2
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 		3 0 1 0.12 0 0
CUI: C3275929
Disease: Superior semicircular canal dehiscence syndrome
Superior semicircular canal dehiscence syndrome 		3 0 1 0.12 0 0
CUI: C3276419
Disease: USHER SYNDROME, TYPE ID/F, DIGENIC
USHER SYNDROME, TYPE ID/F, DIGENIC 		3 0 1 0.12 0 0
CUI: C4022551
Disease: Wide penis
Wide penis 		3 0 1 0.12 0 0
CUI: C4025789
Disease: Psychotic mentation
Psychotic mentation 		3 0 1 0.12 0 0
CUI: C4274947
Disease: Multiple endocrine neoplasia type 4
Multiple endocrine neoplasia type 4 		3 0 1 0.12 0 0
CUI: C0028866
Disease: Oculomotor Nerve Paralysis
Oculomotor Nerve Paralysis 		22 0 3 0.12 0 0
CUI: C1846288
Disease: Recurrent hypoglycemia
Recurrent hypoglycemia 		13 0 2 0.12 0 0
CUI: C1970712
Disease: Multiple Endocrine Neoplasia, Type IV
Multiple Endocrine Neoplasia, Type IV 		13 0 2 0.12 0 0
CUI: C0151639
Disease: Decreased fertility in females
Decreased fertility in females 		23 0 3 0.12 0 0
CUI: C0238114
Disease: Leiomyoma of esophagus
Leiomyoma of esophagus 		4 0 1 0.11 0 0
CUI: C0854021
Disease: Abnormal visual field test
Abnormal visual field test 		4 0 1 0.11 0 0
CUI: C1368066
Disease: islet cell gastrinoma
islet cell gastrinoma 		4 0 1 0.11 0 0
CUI: C1832394
Disease: Deafness, Autosomal Recessive 12
Deafness, Autosomal Recessive 12 		4 0 1 0.11 0 0
CUI: C1844831
Disease: Cleft Palate with Ankyloglossia
Cleft Palate with Ankyloglossia 		4 0 1 0.11 0 0
CUI: C1848634
Disease: USHER SYNDROME, TYPE IIA
USHER SYNDROME, TYPE IIA 		4 0 1 0.11 0 0
CUI: C2931039
Disease: Pancreatic islet cell tumors
Pancreatic islet cell tumors 		4 0 1 0.11 0 0
CUI: C2931208
Disease: Usher syndrome, type 1D
Usher syndrome, type 1D 		4 0 1 0.11 0 0
CUI: C0271578
Disease: Female hypogonadism syndrome
Female hypogonadism syndrome 		25 0 3 0.11 0 0
CUI: C0220744
Disease: Multiple gastrointestinal atresias (disorder)
Multiple gastrointestinal atresias (disorder) 		5 0 1 1.0E-01 0 0
CUI: C0238374
Disease: PITUITARY ADENOMA, NON-SECRETING
PITUITARY ADENOMA, NON-SECRETING 		5 0 1 1.0E-01 0 0
CUI: C0271560
Disease: Lymphocytic hypopituitarism
Lymphocytic hypopituitarism 		5 0 1 1.0E-01 0 0
CUI: C0342410
Disease: Autoimmune Hypophysitis
Autoimmune Hypophysitis 		5 0 1 1.0E-01 0 0