Source: ALL
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: C0442880
Disease: Periungual fibroma
Periungual fibroma 		2 0 2 0.40 0 0
CUI: C1860715
Disease: Giant cell astrocytoma
Giant cell astrocytoma 		2 0 2 0.40 0 0
CUI: C0238399
Disease: Pulmonary lymphangiomyomatosis
Pulmonary lymphangiomyomatosis 		3 0 2 0.33 0 0
CUI: C0266003
Disease: Subungual fibroma
Subungual fibroma 		3 0 2 0.33 0 0
CUI: C1846386
Disease: Focal Cortical Dysplasia of Taylor, Type IIa
Focal Cortical Dysplasia of Taylor, Type IIa 		3 0 2 0.33 0 0
CUI: C1846389
Disease: Focal Cortical Dysplasia of Taylor, Type IIb
Focal Cortical Dysplasia of Taylor, Type IIb 		3 0 2 0.33 0 0
CUI: C1860710
Disease: Achromatic retinal patches
Achromatic retinal patches 		3 0 2 0.33 0 0
CUI: C1968958
Disease: Subependymal nodules
Subependymal nodules 		3 0 2 0.33 0 0
CUI: C1968959
Disease: Cortical tubers
Cortical tubers 		3 0 2 0.33 0 0
CUI: C0242426
Disease: Chylopericardium
Chylopericardium 		4 0 2 0.29 0 0
CUI: C1863411
Disease: Retinal hamartoma
Retinal hamartoma 		4 0 2 0.29 0 0
CUI: C2350234
Disease: Clear-Cell Sugar Tumors
Clear-Cell Sugar Tumors 		5 0 2 0.25 0 0
CUI: C0553558
Disease: Jackknife Seizures
Jackknife Seizures 		6 0 2 0.22 0 0
CUI: C1112324
Disease: Multifocal micronodular pneumocyte hyperplasia
Multifocal micronodular pneumocyte hyperplasia 		6 0 2 0.22 0 0
CUI: C1332852
Disease: Cardiac rhabdomyoma
Cardiac rhabdomyoma 		6 0 2 0.22 0 0
CUI: C1527306
Disease: spasmus nutans
spasmus nutans 		6 0 2 0.22 0 0
CUI: C0157733
Disease: Abnormality of the hair
Abnormality of the hair 		1 0 1 0.20 0 0
CUI: C0399373
Disease: Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism
Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism 		1 0 1 0.20 0 0
CUI: C1302778
Disease: Congenital lymphatic malformation
Congenital lymphatic malformation 		1 0 1 0.20 0 0
CUI: C1860855
Disease: Obliteration of the calvarial diploe
Obliteration of the calvarial diploe 		1 0 1 0.20 0 0
CUI: C1863012
Disease: Amelogenesis Imperfecta, Type IV
Amelogenesis Imperfecta, Type IV 		1 0 1 0.20 0 0
CUI: C4015557
Disease: AMELOGENESIS IMPERFECTA, TYPE IH
AMELOGENESIS IMPERFECTA, TYPE IH 		1 0 1 0.20 0 0
CUI: C4025872
Disease: Abnormality of the mastoid
Abnormality of the mastoid 		1 0 1 0.20 0 0
CUI: C4225394
Disease: AMELOGENESIS IMPERFECTA, TYPE IF
AMELOGENESIS IMPERFECTA, TYPE IF 		1 0 1 0.20 0 0
CUI: C4280782
Disease: Periapical tooth abscess
Periapical tooth abscess 		1 0 1 0.20 0 0