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: C1337036
Disease: Renal Cell Carcinoma Associated with Xp11.2 Translocations/TFE3 Gene Fusions
Renal Cell Carcinoma Associated with Xp11.2 Translocations/TFE3 Gene Fusions 		6 0 3 0.38 0 0
CUI: C2350234
Disease: Clear-Cell Sugar Tumors
Clear-Cell Sugar Tumors 		5 0 2 0.25 0 0
CUI: C0014647
Disease: Giant Cell Epulis
Giant Cell Epulis 		6 0 2 0.22 0 0
CUI: C0266305
Disease: Fused Kidney
Fused Kidney 		1 0 1 0.20 0 0
CUI: C0267166
Disease: Gastroduodenitis
Gastroduodenitis 		1 0 1 0.20 0 0
CUI: C0391816
Disease: Tietz syndrome
Tietz syndrome 		1 0 1 0.20 0 0
CUI: C1368821
Disease: Ovarian Sclerosing Stromal Tumor
Ovarian Sclerosing Stromal Tumor 		1 0 1 0.20 0 0
CUI: C3839062
Disease: Perivascular epithelioid tumor, malignant
Perivascular epithelioid tumor, malignant 		1 0 1 0.20 0 0
CUI: C4310625
Disease: COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS 		1 0 1 0.20 0 0
CUI: C4750999
Disease: Ocular albinism with congenital sensorineural deafness
Ocular albinism with congenital sensorineural deafness 		1 0 1 0.20 0 0
CUI: C0034188
Disease: Pyelonephritis, Xanthogranulomatous
Pyelonephritis, Xanthogranulomatous 		2 0 1 0.17 0 0
CUI: C0078921
Disease: Albinism, Tyrosinase-Negative
Albinism, Tyrosinase-Negative 		2 0 1 0.17 0 0
CUI: C0078922
Disease: Albinism, Tyrosinase-Positive
Albinism, Tyrosinase-Positive 		2 0 1 0.17 0 0
CUI: C0078923
Disease: Albinism, Yellow-Mutant
Albinism, Yellow-Mutant 		2 0 1 0.17 0 0
CUI: C0155096
Disease: Corneal ghost vessels
Corneal ghost vessels 		2 0 1 0.17 0 0
CUI: C0346054
Disease: Verruciform xanthoma of skin
Verruciform xanthoma of skin 		2 0 1 0.17 0 0
CUI: C1332614
Disease: Angiosarcoma of the breast
Angiosarcoma of the breast 		2 0 1 0.17 0 0
CUI: C1333962
Disease: Hepatic Angiomyolipoma
Hepatic Angiomyolipoma 		2 0 1 0.17 0 0
CUI: C1863198
Disease: ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder)
ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder) 		2 0 1 0.17 0 0
CUI: C3152204
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 		2 0 1 0.17 0 0
CUI: C4288080
Disease: UNC13D Deficiency
UNC13D Deficiency 		2 0 1 0.17 0 0
CUI: C4525234
Disease: Xiphophorus Melanoma
Xiphophorus Melanoma 		2 0 1 0.17 0 0
CUI: C1300127
Disease: Perivascular Epithelioid Cell Neoplasms
Perivascular Epithelioid Cell Neoplasms 		31 0 5 0.16 0 0
CUI: C0162375
Disease: Granuloma, Giant Cell Reparative
Granuloma, Giant Cell Reparative 		11 0 2 0.14 0 0
CUI: C0334618
Disease: Malignant granular cell tumor
Malignant granular cell tumor 		3 0 1 0.14 0 0