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: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		88 6387 2 1.9E-02 1 1.6E-04
CUI: C0027651
Disease: Neoplasms
Neoplasms 		10161 1644 18 1.8E-03 1 6.1E-04
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		8621 1641 18 2.1E-03 1 6.1E-04
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		8221 1374 18 2.2E-03 1 7.3E-04
CUI: C0025202
Disease: melanoma
melanoma 		3087 515 15 4.9E-03 1 1.9E-03
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		842 420 1 1.2E-03 1 2.4E-03
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		6243 355 15 2.4E-03 1 2.8E-03
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		2689 322 9 3.3E-03 1 3.1E-03
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		2084 288 9 4.3E-03 1 3.5E-03
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		2667 277 9 3.4E-03 1 3.6E-03
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		507 248 9 1.7E-02 1 4.0E-03
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		2346 222 11 4.7E-03 1 4.5E-03
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		344 186 6 1.7E-02 1 5.4E-03
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability 		251 94 1 3.7E-03 1 1.1E-02
CUI: C0009806
Disease: Constipation
Constipation 		424 57 5 1.1E-02 1 1.8E-02
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
Adrenal Gland Pheochromocytoma 		416 50 9 2.1E-02 1 2.0E-02
CUI: C0027960
Disease: Nevus
Nevus 		125 43 2 1.4E-02 1 2.3E-02
CUI: C0026010
Disease: Microphthalmos
Microphthalmos 		337 40 2 5.7E-03 1 2.5E-02
CUI: C0030421
Disease: Paraganglioma
Paraganglioma 		165 36 6 3.4E-02 1 2.8E-02
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		407 35 2 4.7E-03 1 2.9E-02
CUI: C0027962
Disease: Melanocytic nevus
Melanocytic nevus 		297 33 5 1.6E-02 1 3.0E-02
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		192 26 1 4.8E-03 1 3.8E-02
CUI: C1860339
Disease: WAARDENBURG SYNDROME, TYPE IIA
WAARDENBURG SYNDROME, TYPE IIA 		7 26 2 8.7E-02 1 3.8E-02
CUI: C1456781
Disease: Benign melanocytic nevus
Benign melanocytic nevus 		122 20 2 1.4E-02 1 5.0E-02
CUI: C1849452
Disease: SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder)
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder) 		0 13 0 0 1 7.7E-02