Source: INFERRED ×
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: C0042341
Disease: Varicocele
Varicocele 		3 0 2 0.29 0 0
CUI: C0391826
Disease: Lhermitte-Duclos disease
Lhermitte-Duclos disease 		3 0 2 0.29 0 0
CUI: C0858252
Disease: Breast adenocarcinoma
Breast adenocarcinoma 		3 0 2 0.29 0 0
CUI: C1834711
Disease: CEREBELLOPARENCHYMAL DISORDER VI
CEREBELLOPARENCHYMAL DISORDER VI 		3 0 2 0.29 0 0
CUI: C1834712
Disease: Cerebellar Granule Cell Hypertrophy and Megalencephaly
Cerebellar Granule Cell Hypertrophy and Megalencephaly 		3 0 2 0.29 0 0
CUI: C1866376
Disease: Pten Hamartoma Tumor Syndrome With Granular Cell Tumor
Pten Hamartoma Tumor Syndrome With Granular Cell Tumor 		3 0 2 0.29 0 0
CUI: C1866398
Disease: Proteus-Like Syndrome (disorder)
Proteus-Like Syndrome (disorder) 		3 0 2 0.29 0 0
CUI: C1959582
Disease: PTEN Hamartoma Tumor Syndrome
PTEN Hamartoma Tumor Syndrome 		3 0 2 0.29 0 0
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
NEVUS, EPIDERMAL (disorder) 		8 0 3 0.27 0 0
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		4 98 2 0.25 1 9.7E-03
CUI: C1854417
Disease: Postnatal macrocephaly
Postnatal macrocephaly 		4 0 2 0.25 0 0
CUI: C1859896
Disease: Progressive macrocephaly
Progressive macrocephaly 		5 0 2 0.22 0 0
CUI: C4022025
Disease: Asymmetric growth
Asymmetric growth 		6 0 2 0.20 0 0
CUI: C0265552
Disease: Congenital macrodactylia
Congenital macrodactylia 		7 0 2 0.18 0 0
CUI: C0431391
Disease: Hemimegalencephaly
Hemimegalencephaly 		14 0 3 0.18 0 0
CUI: C0008073
Disease: Developmental Disabilities
Developmental Disabilities 		1 0 1 0.17 0 0
CUI: C0037284
Disease: Skin lesion
Skin lesion 		1 0 1 0.17 0 0
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases 		1 0 1 0.17 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 0 1 0.17 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 0 1 0.17 0 0
CUI: C0221273
Disease: Juvenile polyp
Juvenile polyp 		1 0 1 0.17 0 0
CUI: C0265326
Disease: Bannayan-Riley-Ruvalcaba Syndrome
Bannayan-Riley-Ruvalcaba Syndrome 		1 0 1 0.17 0 0
CUI: C0266166
Disease: Congenital duplication of intestine
Congenital duplication of intestine 		1 0 1 0.17 0 0
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 1 1 0.17 1 0.17
CUI: C0343082
Disease: Senile angioma
Senile angioma 		1 0 1 0.17 0 0