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: C0751489
Disease: Adult Sandhoff Disease
Adult Sandhoff Disease 		2 0 2 0.40 0 0
CUI: C0751490
Disease: Infantile Sandhoff Disease
Infantile Sandhoff Disease 		2 0 2 0.40 0 0
CUI: C0751491
Disease: Juvenile Sandhoff Disease
Juvenile Sandhoff Disease 		2 0 2 0.40 0 0
CUI: C1848920
Disease: GM2-ganglioside accumulation
GM2-ganglioside accumulation 		2 0 2 0.40 0 0
CUI: C2874270
Disease: GM2-GANGLIOSIDOSIS, ADULT
GM2-GANGLIOSIDOSIS, ADULT 		2 0 2 0.40 0 0
CUI: C0017083
Disease: Gangliosidoses
Gangliosidoses 		6 0 3 0.38 0 0
CUI: C1848922
Disease: Hexosaminidase alpha-Subunit Deficiency (Variant B)
Hexosaminidase alpha-Subunit Deficiency (Variant B) 		4 0 2 0.29 0 0
CUI: C2749283
Disease: Gm2-Gangliosidosis, Variant B1
Gm2-Gangliosidosis, Variant B1 		4 0 2 0.29 0 0
CUI: C2216370
Disease: Cherry red spot of the macula
Cherry red spot of the macula 		9 0 3 0.27 0 0
CUI: C0268274
Disease: Gangliosidoses, GM2
Gangliosidoses, GM2 		18 0 4 0.21 0 0
CUI: C0268276
Disease: Juvenile GM 2 gangliosidosis
Juvenile GM 2 gangliosidosis 		1 0 1 0.20 0 0
CUI: C0268278
Disease: Infantile GM 2 gangliosidosis
Infantile GM 2 gangliosidosis 		1 0 1 0.20 0 0
CUI: C0282220
Disease: Amaurotic Familial Idiocy
Amaurotic Familial Idiocy 		1 0 1 0.20 0 0
CUI: C1848913
Disease: Tay-Sachs Disease, Juvenile
Tay-Sachs Disease, Juvenile 		1 0 1 0.20 0 0
CUI: C1848914
Disease: Hexosaminidase A Deficiency, Adult Type
Hexosaminidase A Deficiency, Adult Type 		1 0 1 0.20 0 0
CUI: C1849320
Disease: Sandhoff Disease, Adult Type
Sandhoff Disease, Adult Type 		1 0 1 0.20 0 0
CUI: C1849321
Disease: Sandhoff Disease, Juvenile Type
Sandhoff Disease, Juvenile Type 		1 0 1 0.20 0 0
CUI: C1849322
Disease: Sandhoff Disease, Infantile Type
Sandhoff Disease, Infantile Type 		1 0 1 0.20 0 0
CUI: C2713499
Disease: Total Hexosaminidase Deficiency
Total Hexosaminidase Deficiency 		1 0 1 0.20 0 0
CUI: C2930923
Disease: N-Acetylneuraminic acid storage disease
N-Acetylneuraminic acid storage disease 		1 0 1 0.20 0 0
CUI: C4016988
Disease: GM2-GANGLIOSIDOSIS, CHRONIC
GM2-GANGLIOSIDOSIS, CHRONIC 		1 0 1 0.20 0 0
CUI: C4017633
Disease: HEXA, CZECHOSLOVAKIAN ALLELE PHENOTYPE
HEXA, CZECHOSLOVAKIAN ALLELE PHENOTYPE 		1 0 1 0.20 0 0
CUI: C4310842
Disease: SANDHOFF DISEASE, CHRONIC
SANDHOFF DISEASE, CHRONIC 		1 0 1 0.20 0 0
CUI: C4310843
Disease: TAY-SACHS DISEASE, JUVENILE/ADULT
TAY-SACHS DISEASE, JUVENILE/ADULT 		1 0 1 0.20 0 0
CUI: C4310890
Disease: GM2-GANGLIOSIDOSIS, SUBACUTE
GM2-GANGLIOSIDOSIS, SUBACUTE 		1 0 1 0.20 0 0