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: 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
Perivascular epithelioid tumor, malignant
1 0 1 0.20 0 0
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS
1 0 1 0.20 0 0
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
ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder)
2 0 1 0.17 0 0
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: C0334618
Disease: Malignant granular cell tumor
Malignant granular cell tumor
3 0 1 0.14 0 0
CUI: C0521515
Disease: Calcific tendinitis
Calcific tendinitis
3 0 1 0.14 0 0
ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder)
3 0 1 0.14 0 0
Liver Epithelioid Hemangioendothelioma
3 0 1 0.14 0 0
CUI: C2700405
Disease: WAARDENBURG SYNDROME, TYPE IIE
WAARDENBURG SYNDROME, TYPE IIE
3 0 1 0.14 0 0
Multinucleate cell angiohistiocytoma
3 0 1 0.14 0 0