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: C0391826
Disease: Lhermitte-Duclos disease
Lhermitte-Duclos disease
3 58 3 0.75 56 0.56
CUI: C1834711
Disease: CEREBELLOPARENCHYMAL DISORDER VI
CEREBELLOPARENCHYMAL DISORDER VI
3 56 3 0.75 56 0.57
Cerebellar Granule Cell Hypertrophy and Megalencephaly
3 56 3 0.75 56 0.57
Pten Hamartoma Tumor Syndrome With Granular Cell Tumor
3 56 3 0.75 56 0.57
CUI: C1866398
Disease: Proteus-Like Syndrome (disorder)
Proteus-Like Syndrome (disorder)
3 56 3 0.75 56 0.57
CUI: C1959582
Disease: PTEN Hamartoma Tumor Syndrome
PTEN Hamartoma Tumor Syndrome
3 193 3 0.75 63 0.28
CUI: C0042341
Disease: Varicocele
Varicocele
3 0 2 0.40 0 0
CUI: C4025896
Disease: Abnormality of the penis
Abnormality of the penis
8 0 3 0.33 0 0
CUI: C1859896
Disease: Progressive macrocephaly
Progressive macrocephaly
5 0 2 0.29 0 0
CUI: C4021849
Disease: Conjunctival hamartoma
Conjunctival hamartoma
10 0 3 0.27 0 0
CUI: C0008073
Disease: Developmental Disabilities
Developmental Disabilities
1 1 1 0.25 1 1.0E-02
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
1 0 1 0.25 0 0
CUI: C0037284
Disease: Skin lesion
Skin lesion
1 1 1 0.25 1 1.0E-02
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases
1 1 1 0.25 1 1.0E-02
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers
1 0 1 0.25 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe
1 1 1 0.25 1 1.0E-02
CUI: C0221273
Disease: Juvenile polyp
Juvenile polyp
1 1 1 0.25 1 1.0E-02
CUI: C0265326
Disease: Bannayan-Riley-Ruvalcaba Syndrome
Bannayan-Riley-Ruvalcaba Syndrome
1 1 1 0.25 1 1.0E-02
CUI: C0266166
Disease: Congenital duplication of intestine
Congenital duplication of intestine
1 1 1 0.25 1 1.0E-02
CUI: C0343082
Disease: Senile angioma
Senile angioma
1 0 1 0.25 0 0
CUI: C0424939
Disease: Learning difficulties
Learning difficulties
6 6 2 0.25 1 9.7E-03
CUI: C0457193
Disease: Soft tissue mass
Soft tissue mass
1 0 1 0.25 0 0
CUI: C1262299
Disease: Oral wart
Oral wart
1 1 1 0.25 1 1.0E-02
CUI: C1333600
Disease: Hereditary Malignant Neoplasm
Hereditary Malignant Neoplasm
1 0 1 0.25 0 0
CUI: C1854416
Disease: MACROCEPHALY/AUTISM SYNDROME
MACROCEPHALY/AUTISM SYNDROME
1 21 1 0.25 9 8.2E-02