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: C0700198
Disease: Pulmonary aspiration
Pulmonary aspiration 		13 0 13 1.00 0 0
CUI: C1963221
Disease: Aspiration, CTCAE
Aspiration, CTCAE 		13 0 13 1.00 0 0
CUI: C2827071
Disease: Unintentional Material Aspiration
Unintentional Material Aspiration 		13 0 13 1.00 0 0
CUI: C2712334
Disease: Actual Aspiration
Actual Aspiration 		18 0 13 0.72 0 0
CUI: C0396064
Disease: Bowing of vocal cord
Bowing of vocal cord 		2 0 2 0.15 0 0
CUI: C0748605
Disease: nocturnal seizures
nocturnal seizures 		2 0 2 0.15 0 0
CUI: C1848920
Disease: GM2-ganglioside accumulation
GM2-ganglioside accumulation 		2 0 2 0.15 0 0
CUI: C1740801
Disease: Exaggerated startle response
Exaggerated startle response 		18 0 4 0.15 0 0
CUI: C0393719
Disease: Nocturnal epilepsy
Nocturnal epilepsy 		4 0 2 0.13 0 0
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		5 0 2 0.12 0 0
CUI: C1835614
Disease: Hereditary Hyperexplexia
Hereditary Hyperexplexia 		7 0 2 0.11 0 0
CUI: C1853486
Disease: Widow's peak
Widow's peak 		9 0 2 1.0E-01 0 0
CUI: C2216370
Disease: Cherry red spot of the macula
Cherry red spot of the macula 		9 0 2 1.0E-01 0 0
CUI: C0234853
Disease: Facial grimacing
Facial grimacing 		10 0 2 9.5E-02 0 0
CUI: C4025750
Disease: Abnormality of the nasopharynx
Abnormality of the nasopharynx 		10 0 2 9.5E-02 0 0
CUI: C0266054
Disease: Premature tooth eruption
Premature tooth eruption 		12 0 2 8.7E-02 0 0
CUI: C0234166
Disease: Hyperexplexia
Hyperexplexia 		13 0 2 8.3E-02 0 0
CUI: C1801950
Disease: Opitz-G syndrome, type 2
Opitz-G syndrome, type 2 		13 0 2 8.3E-02 0 0
CUI: C0239043
Disease: Difficulty chewing
Difficulty chewing 		14 0 2 8.0E-02 0 0
CUI: C0268276
Disease: Juvenile GM 2 gangliosidosis
Juvenile GM 2 gangliosidosis 		1 0 1 7.7E-02 0 0
CUI: C0282220
Disease: Amaurotic Familial Idiocy
Amaurotic Familial Idiocy 		1 0 1 7.7E-02 0 0
CUI: C1834042
Disease: Hypoplasia of facial musculature
Hypoplasia of facial musculature 		1 0 1 7.7E-02 0 0
CUI: C1842898
Disease: Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency 		1 0 1 7.7E-02 0 0
CUI: C1848913
Disease: Tay-Sachs Disease, Juvenile
Tay-Sachs Disease, Juvenile 		1 0 1 7.7E-02 0 0
CUI: C1848914
Disease: Hexosaminidase A Deficiency, Adult Type
Hexosaminidase A Deficiency, Adult Type 		1 0 1 7.7E-02 0 0