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: C3887520
Disease: Childhood Pineoblastoma
Childhood Pineoblastoma
13 0 3 7.3E-02 0 0
CUI: C1856659
Disease: Polysplenia
Polysplenia
15 0 3 7.0E-02 0 0
CUI: C0334488
Disease: Clear cell sarcoma of kidney
Clear cell sarcoma of kidney
31 0 4 6.9E-02 0 0
CUI: C0221273
Disease: Juvenile polyp
Juvenile polyp
16 0 3 6.8E-02 0 0
CUI: C0685695
Disease: Abnormal lung lobation
Abnormal lung lobation
32 0 4 6.8E-02 0 0
CUI: C1704327
Disease: Bone Sarcoma
Bone Sarcoma
32 0 4 6.8E-02 0 0
CUI: C1367536
Disease: Nasopharyngeal Angiofibroma
Nasopharyngeal Angiofibroma
17 0 3 6.7E-02 0 0
Serous Tubal Intraepithelial Carcinoma
33 0 4 6.7E-02 0 0
CUI: C0206661
Disease: Gonadoblastoma
Gonadoblastoma
34 0 4 6.6E-02 0 0
CUI: C0278803
Disease: Adenocarcinoma of small intestine
Adenocarcinoma of small intestine
34 0 4 6.6E-02 0 0
CUI: C0205898
Disease: pineoblastoma
pineoblastoma
18 0 3 6.5E-02 0 0
CUI: C1266047
Disease: Fetal adenocarcinoma
Fetal adenocarcinoma
2 0 2 6.5E-02 0 0
CUI: C1708045
Disease: Fetal Lung Adenocarcinoma
Fetal Lung Adenocarcinoma
2 0 2 6.5E-02 0 0
CUI: C1839277
Disease: Submucous cleft lip
Submucous cleft lip
2 0 2 6.5E-02 0 0
CUI: C1839279
Disease: Six lumbar vertebrae
Six lumbar vertebrae
2 0 2 6.5E-02 0 0
Two carpal ossification centers present at birth
2 0 2 6.5E-02 0 0
CUI: C1842124
Disease: BRANCHIOOTIC SYNDROME 3 (disorder)
BRANCHIOOTIC SYNDROME 3 (disorder)
2 0 2 6.5E-02 0 0
CUI: C2986703
Disease: Overgrowth Syndrome
Overgrowth Syndrome
36 0 4 6.3E-02 0 0
CUI: C0206656
Disease: Embryonal Rhabdomyosarcoma
Embryonal Rhabdomyosarcoma
121 0 9 6.3E-02 0 0
CUI: C0334307
Disease: Tubulovillous adenoma
Tubulovillous adenoma
20 0 3 6.2E-02 0 0
CUI: C0334401
Disease: Malignant Granulosa Cell Tumor
Malignant Granulosa Cell Tumor
3 0 2 6.2E-02 0 0
CUI: C0750887
Disease: Adrenal Cancer
Adrenal Cancer
20 0 3 6.2E-02 0 0
CUI: C1266082
Disease: Atypical medullary carcinoma
Atypical medullary carcinoma
3 0 2 6.2E-02 0 0
CUI: C1839269
Disease: Duplication of renal pelvis
Duplication of renal pelvis
3 0 2 6.2E-02 0 0
Chromosomal mosaicism due to mitotic instability
3 0 2 6.2E-02 0 0