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: C0751278
Disease: Metachromatic Leukodystrophy, Infant
Metachromatic Leukodystrophy, Infant 		2 10 2 1.00 1 7.1E-02
CUI: C0011103
Disease: Decerebrate State
Decerebrate State 		3 0 2 0.67 0 0
CUI: C0751279
Disease: Metachromatic Leukodystrophy, Adult-Type (disorder)
Metachromatic Leukodystrophy, Adult-Type (disorder) 		3 7 2 0.67 3 0.33
CUI: C4024961
Disease: Metachromatic leukodystrophy variant
Metachromatic leukodystrophy variant 		3 0 2 0.67 0 0
CUI: C4025350
Disease: Abnormality of glycosphingolipid metabolism
Abnormality of glycosphingolipid metabolism 		3 0 2 0.67 0 0
CUI: C0221069
Disease: Anterior Spinal Artery Syndrome
Anterior Spinal Artery Syndrome 		1 0 1 0.50 0 0
CUI: C0268262
Disease: Metachromatic Leukodystrophy due to Saposin B Deficiency
Metachromatic Leukodystrophy due to Saposin B Deficiency 		1 0 1 0.50 0 0
CUI: C0392322
Disease: Undifferentiated schizophrenia
Undifferentiated schizophrenia 		1 0 1 0.50 0 0
CUI: C0401067
Disease: Unilateral inguinal hernia NOS
Unilateral inguinal hernia NOS 		1 0 1 0.50 0 0
CUI: C0520559
Disease: Numbness of tongue
Numbness of tongue 		1 0 1 0.50 0 0
CUI: C0740406
Disease: Incarcerated hernia
Incarcerated hernia 		1 0 1 0.50 0 0
CUI: C1263726
Disease: Sulfatiduria
Sulfatiduria 		1 0 1 0.50 0 0
CUI: C1328500
Disease: Intraoperative hypertension
Intraoperative hypertension 		1 0 1 0.50 0 0
CUI: C1706192
Disease: Sulfatidosis
Sulfatidosis 		1 0 1 0.50 0 0
CUI: C1855255
Disease: Pseudoarylsulfatase A Deficiency
Pseudoarylsulfatase A Deficiency 		1 0 1 0.50 0 0
CUI: C1864651
Disease: GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY
GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY 		1 0 1 0.50 0 0
CUI: C4017091
Disease: ARYLSULFATASE A PSEUDODEFICIENCY
ARYLSULFATASE A PSEUDODEFICIENCY 		1 0 1 0.50 0 0
CUI: C4017093
Disease: METACHROMATIC LEUKODYSTROPHY, LATE-ONSET
METACHROMATIC LEUKODYSTROPHY, LATE-ONSET 		1 0 1 0.50 0 0
CUI: C4017094
Disease: METACHROMATIC LEUKODYSTROPHY, SEVERE
METACHROMATIC LEUKODYSTROPHY, SEVERE 		1 0 1 0.50 0 0
CUI: C4017095
Disease: ARYLSULFATASE A PSEUDODEFICIENCY, SEVERE
ARYLSULFATASE A PSEUDODEFICIENCY, SEVERE 		1 0 1 0.50 0 0
CUI: C4017096
Disease: ARYLSULFATASE A PSEUDODEFICIENCY, INTERMEDIATE
ARYLSULFATASE A PSEUDODEFICIENCY, INTERMEDIATE 		1 0 1 0.50 0 0
CUI: C4017847
Disease: METACHROMATIC LEUKODYSTROPHY, MILD
METACHROMATIC LEUKODYSTROPHY, MILD 		1 0 1 0.50 0 0
CUI: C4022658
Disease: Punctate periventricular T2 hyperintense foci
Punctate periventricular T2 hyperintense foci 		4 0 2 0.50 0 0
CUI: C4023177
Disease: Increased cerebral lipofuscin
Increased cerebral lipofuscin 		1 0 1 0.50 0 0
CUI: C0917808
Disease: Vegetative State
Vegetative State 		5 0 2 0.40 0 0