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: C4523846
Disease: MSI-high
MSI-high 		83 9 29 0.32 2 0.22
CUI: C1334003
Disease: Barretts esophagus with high grade dysplasia
Barretts esophagus with high grade dysplasia 		12 0 9 0.23 0 0
CUI: C0240164
Disease: Squamous Papilloma of the Larynx
Squamous Papilloma of the Larynx 		18 0 10 0.22 0 0
CUI: C1881254
Disease: Inverted Squamous Cell Papilloma
Inverted Squamous Cell Papilloma 		46 0 15 0.22 0 0
CUI: C0271375
Disease: Fourth cranial nerve paresis
Fourth cranial nerve paresis 		13 0 9 0.22 0 0
CUI: C1333383
Disease: Encapsulated Thymoma
Encapsulated Thymoma 		8 0 8 0.22 0 0
CUI: C0206721
Disease: Inverted Papilloma
Inverted Papilloma 		51 0 15 0.21 0 0
CUI: C0334431
Disease: Melanocytoma
Melanocytoma 		18 3 9 0.20 2 0.67
CUI: C4525405
Disease: Eyelid Sebaceous Gland Carcinoma
Eyelid Sebaceous Gland Carcinoma 		18 0 9 0.20 0 0
CUI: C1970712
Disease: Multiple Endocrine Neoplasia, Type IV
Multiple Endocrine Neoplasia, Type IV 		13 0 8 0.19 0 0
CUI: C0024814
Disease: Marinesco-Sjogren syndrome
Marinesco-Sjogren syndrome 		133 8 27 0.19 2 0.25
CUI: C1847319
Disease: PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA
PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA 		20 0 9 0.19 0 0
CUI: C0259770
Disease: Epithelial inclusion cyst
Epithelial inclusion cyst 		14 0 8 0.19 0 0
CUI: C2676191
Disease: PITUITARY ADENOMA, FAMILIAL ISOLATED (disorder)
PITUITARY ADENOMA, FAMILIAL ISOLATED (disorder) 		16 0 8 0.18 0 0
CUI: C1860707
Disease: TUBEROUS SCLEROSIS 2 (disorder)
TUBEROUS SCLEROSIS 2 (disorder) 		43 0 12 0.18 0 0
CUI: C0265325
Disease: Turcot syndrome (disorder)
Turcot syndrome (disorder) 		77 75 17 0.18 2 2.7E-02
CUI: C0334292
Disease: Tubular adenoma
Tubular adenoma 		17 0 8 0.17 0 0
CUI: C1334647
Disease: Maxillary Sinus Squamous Cell Carcinoma
Maxillary Sinus Squamous Cell Carcinoma 		24 0 9 0.17 0 0
CUI: C0334581
Disease: Gemistocytic astrocytoma
Gemistocytic astrocytoma 		45 0 12 0.17 0 0
CUI: C0280451
Disease: de novo myelodysplastic syndromes
de novo myelodysplastic syndromes 		27 0 9 0.16 0 0
CUI: C4024989
Disease: Hereditary nonpolyposis colorectal carcinoma
Hereditary nonpolyposis colorectal carcinoma 		28 5 9 0.16 2 0.40
CUI: C1708604
Disease: Keratocystic Odontogenic Tumor
Keratocystic Odontogenic Tumor 		59 2 13 0.16 2 1.00
CUI: C2678061
Disease: SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT 		30 0 9 0.16 0 0
CUI: C1707440
Disease: Colorectal Signet Ring Cell Carcinoma
Colorectal Signet Ring Cell Carcinoma 		8 0 6 0.15 0 0
CUI: C0221273
Disease: Juvenile polyp
Juvenile polyp 		16 0 7 0.15 0 0