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: C3151302
Disease: Chromosome 13q14 deletion syndrome
Chromosome 13q14 deletion syndrome
1 0 1 1.00 0 0
CUI: C1704237
Disease: Trichodiscoma
Trichodiscoma
2 0 1 0.50 0 0
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
2 0 1 0.50 0 0
WOOLLY HAIR, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT HYPOTRICHOSIS
2 0 1 0.50 0 0
CUI: C1867289
Disease: Retinal calcification
Retinal calcification
2 0 1 0.50 0 0
Vulvar Adenocarcinoma of Mammary Gland Type
2 0 1 0.50 0 0
CUI: C0854915
Disease: Retinoblastoma unilateral
Retinoblastoma unilateral
3 0 1 0.33 0 0
CUI: C1334266
Disease: Intraurothelial Neoplasia
Intraurothelial Neoplasia
3 0 1 0.33 0 0
CUI: C2608045
Disease: Trilateral Retinoblastoma
Trilateral Retinoblastoma
3 0 1 0.33 0 0
Abnormality of the tibial metaphysis
3 0 1 0.33 0 0
CUI: C0152458
Disease: Leukocoria
Leukocoria
4 0 1 0.25 0 0
Abnormality of the femoral metaphysis
4 0 1 0.25 0 0
CUI: C0854914
Disease: Retinoblastoma bilateral
Retinoblastoma bilateral
6 0 1 0.17 0 0
CUI: C0751484
Disease: Sporadic Retinoblastoma
Sporadic Retinoblastoma
7 0 1 0.14 0 0
CUI: C2930975
Disease: Acute erythroleukemia - M6a subtype
Acute erythroleukemia - M6a subtype
8 0 1 0.12 0 0
CUI: C2930976
Disease: Acute myeloid leukemia FAB-M6
Acute myeloid leukemia FAB-M6
8 0 1 0.12 0 0
CUI: C2930977
Disease: Acute erythroleukemia - M6b subtype
Acute erythroleukemia - M6b subtype
8 0 1 0.12 0 0
CUI: C0346011
Disease: Fibrofolliculoma
Fibrofolliculoma
10 0 1 1.0E-01 0 0
CUI: C0496836
Disease: Malignant tumor of eye
Malignant tumor of eye
11 0 1 9.1E-02 0 0
CUI: C0042909
Disease: Vitreous Hemorrhage
Vitreous Hemorrhage
12 0 1 8.3E-02 0 0
CUI: C0751483
Disease: Familial Retinoblastoma
Familial Retinoblastoma
12 0 1 8.3E-02 0 0
CUI: C0281332
Disease: Adult Pineoblastoma
Adult Pineoblastoma
13 0 1 7.7E-02 0 0
CUI: C2930974
Disease: Acute erythroleukemia
Acute erythroleukemia
13 0 1 7.7E-02 0 0
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8
13 0 1 7.7E-02 0 0
CUI: C3887520
Disease: Childhood Pineoblastoma
Childhood Pineoblastoma
13 0 1 7.7E-02 0 0