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: 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
CUI: C1854990
Disease: Molybdenum Cofactor Deficiency, Complementation Group C
Molybdenum Cofactor Deficiency, Complementation Group C 		1 0 1 7.7E-02 0 0
CUI: C3807521
Disease: AMYOTROPHIC LATERAL SCLEROSIS 21
AMYOTROPHIC LATERAL SCLEROSIS 21 		1 0 1 7.7E-02 0 0
CUI: C4014538
Disease: ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder
ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder 		1 0 1 7.7E-02 0 0
CUI: C4016988
Disease: GM2-GANGLIOSIDOSIS, CHRONIC
GM2-GANGLIOSIDOSIS, CHRONIC 		1 0 1 7.7E-02 0 0
CUI: C4017633
Disease: HEXA, CZECHOSLOVAKIAN ALLELE PHENOTYPE
HEXA, CZECHOSLOVAKIAN ALLELE PHENOTYPE 		1 0 1 7.7E-02 0 0
CUI: C4021055
Disease: Absent muscle fiber merosin
Absent muscle fiber merosin 		1 0 1 7.7E-02 0 0
CUI: C4025101
Disease: Imperfect vocal cord adduction
Imperfect vocal cord adduction 		1 0 1 7.7E-02 0 0
CUI: C4255079
Disease: Familial Hyperekplexia
Familial Hyperekplexia 		1 0 1 7.7E-02 0 0
CUI: C4310843
Disease: TAY-SACHS DISEASE, JUVENILE/ADULT
TAY-SACHS DISEASE, JUVENILE/ADULT 		1 0 1 7.7E-02 0 0
CUI: C4310890
Disease: GM2-GANGLIOSIDOSIS, SUBACUTE
GM2-GANGLIOSIDOSIS, SUBACUTE 		1 0 1 7.7E-02 0 0
CUI: C4310892
Disease: BETA-HEXOSAMINIDASE A, PSEUDODEFICIENCY OF
BETA-HEXOSAMINIDASE A, PSEUDODEFICIENCY OF 		1 0 1 7.7E-02 0 0
CUI: C4748327
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23
MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23 		1 0 1 7.7E-02 0 0
CUI: C0014736
Disease: Erysipelothrix infection
Erysipelothrix infection 		2 0 1 7.1E-02 0 0
CUI: C0240017
Disease: Intercostal muscle weakness
Intercostal muscle weakness 		2 0 1 7.1E-02 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: C0796179
Disease: Teebi syndrome
Teebi syndrome 		2 0 1 7.1E-02 0 0
CUI: C1542327
Disease: Fetus or newborn affected by alcohol transmitted via placenta or breast milk
Fetus or newborn affected by alcohol transmitted via placenta or breast milk 		2 0 1 7.1E-02 0 0
CUI: C1838348
Disease: Oculomaxillofacial dysostosis
Oculomaxillofacial dysostosis 		2 0 1 7.1E-02 0 0