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: C1333383
Disease: Encapsulated Thymoma
Encapsulated Thymoma 		8 0 8 0.32 0 0
CUI: C0152264
Disease: Familial erythrocytosis
Familial erythrocytosis 		17 0 10 0.31 0 0
CUI: C1334003
Disease: Barretts esophagus with high grade dysplasia
Barretts esophagus with high grade dysplasia 		12 0 8 0.28 0 0
CUI: C0271375
Disease: Fourth cranial nerve paresis
Fourth cranial nerve paresis 		13 0 8 0.27 0 0
CUI: C1970712
Disease: Multiple Endocrine Neoplasia, Type IV
Multiple Endocrine Neoplasia, Type IV 		13 0 8 0.27 0 0
CUI: C0259770
Disease: Epithelial inclusion cyst
Epithelial inclusion cyst 		14 0 8 0.26 0 0
CUI: C1847319
Disease: PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA
PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA 		20 0 9 0.25 0 0
CUI: C2676191
Disease: PITUITARY ADENOMA, FAMILIAL ISOLATED (disorder)
PITUITARY ADENOMA, FAMILIAL ISOLATED (disorder) 		16 0 8 0.24 0 0
CUI: C0280451
Disease: de novo myelodysplastic syndromes
de novo myelodysplastic syndromes 		27 0 10 0.24 0 0
CUI: C0240164
Disease: Squamous Papilloma of the Larynx
Squamous Papilloma of the Larynx 		18 0 8 0.23 0 0
CUI: C0334431
Disease: Melanocytoma
Melanocytoma 		18 0 8 0.23 0 0
CUI: C4525405
Disease: Eyelid Sebaceous Gland Carcinoma
Eyelid Sebaceous Gland Carcinoma 		18 0 8 0.23 0 0
CUI: C4551637
Disease: Erythrocytosis familial, 1
Erythrocytosis familial, 1 		29 14 10 0.23 1 4.8E-02
CUI: C1858592
Disease: Carney Triad
Carney Triad 		25 0 9 0.22 0 0
CUI: C0233746
Disease: Perceptual disturbance
Perceptual disturbance 		5 0 5 0.20 0 0
CUI: C1334647
Disease: Maxillary Sinus Squamous Cell Carcinoma
Maxillary Sinus Squamous Cell Carcinoma 		24 0 8 0.20 0 0
CUI: C0021151
Disease: Incipient Schizophrenia
Incipient Schizophrenia 		6 0 5 0.19 0 0
CUI: C0730315
Disease: Acute central serous chorioretinopathy
Acute central serous chorioretinopathy 		7 0 5 0.19 0 0
CUI: C2678061
Disease: SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT 		30 0 8 0.17 0 0
CUI: C0240805
Disease: Prodrome
Prodrome 		10 0 5 0.17 0 0
CUI: C1846006
Disease: Ectodermal dysplasia, hypohidrotic, with immune deficiency
Ectodermal dysplasia, hypohidrotic, with immune deficiency 		10 0 5 0.17 0 0
CUI: C0032461
Disease: Polycythemia
Polycythemia 		82 22 14 0.15 3 0.11
CUI: C1854310
Disease: Hypotrichosis simplex
Hypotrichosis simplex 		37 0 8 0.15 0 0
CUI: C4524257
Disease: MSI-low
MSI-low 		37 0 8 0.15 0 0
CUI: C0079747
Disease: Low Grade Lymphoma (neoplasm)
Low Grade Lymphoma (neoplasm) 		39 0 8 0.14 0 0