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: C0221069
Disease: Anterior Spinal Artery Syndrome
Anterior Spinal Artery Syndrome 		1 0 1 9.1E-02 0 0
CUI: C0268262
Disease: Metachromatic Leukodystrophy due to Saposin B Deficiency
Metachromatic Leukodystrophy due to Saposin B Deficiency 		1 0 1 9.1E-02 0 0
CUI: C0392322
Disease: Undifferentiated schizophrenia
Undifferentiated schizophrenia 		1 0 1 9.1E-02 0 0
CUI: C0393560
Disease: Vascular Dementia, Acute Onset
Vascular Dementia, Acute Onset 		1 0 1 9.1E-02 0 0
CUI: C0401067
Disease: Unilateral inguinal hernia NOS
Unilateral inguinal hernia NOS 		1 0 1 9.1E-02 0 0
CUI: C0423640
Disease: Right Flank Pain
Right Flank Pain 		1 0 1 9.1E-02 0 0
CUI: C0520559
Disease: Numbness of tongue
Numbness of tongue 		1 0 1 9.1E-02 0 0
CUI: C0521527
Disease: Shortened trunk
Shortened trunk 		1 0 1 9.1E-02 0 0
CUI: C0600359
Disease: Arteriosclerotic Dementia
Arteriosclerotic Dementia 		1 0 1 9.1E-02 0 0
CUI: C0740406
Disease: Incarcerated hernia
Incarcerated hernia 		1 0 1 9.1E-02 0 0
CUI: C0860475
Disease: Lactose intolerant
Lactose intolerant 		1 0 1 9.1E-02 0 0
CUI: C1263726
Disease: Sulfatiduria
Sulfatiduria 		1 0 1 9.1E-02 0 0
CUI: C1328500
Disease: Intraoperative hypertension
Intraoperative hypertension 		1 0 1 9.1E-02 0 0
CUI: C1332860
Disease: Cauda Equina Paraganglioma
Cauda Equina Paraganglioma 		1 0 1 9.1E-02 0 0
CUI: C1706192
Disease: Sulfatidosis
Sulfatidosis 		1 0 1 9.1E-02 0 0
CUI: C1849320
Disease: Sandhoff Disease, Adult Type
Sandhoff Disease, Adult Type 		1 0 1 9.1E-02 0 0
CUI: C1849321
Disease: Sandhoff Disease, Juvenile Type
Sandhoff Disease, Juvenile Type 		1 0 1 9.1E-02 0 0
CUI: C1849322
Disease: Sandhoff Disease, Infantile Type
Sandhoff Disease, Infantile Type 		1 0 1 9.1E-02 0 0
CUI: C1855255
Disease: Pseudoarylsulfatase A Deficiency
Pseudoarylsulfatase A Deficiency 		1 0 1 9.1E-02 0 0
CUI: C1860972
Disease: GENIOSPASM 1
GENIOSPASM 1 		1 0 1 9.1E-02 0 0
CUI: C1864651
Disease: GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY
GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY 		1 0 1 9.1E-02 0 0
CUI: C1868633
Disease: Paragangliomas with Sensorineural Hearing Loss
Paragangliomas with Sensorineural Hearing Loss 		1 0 1 9.1E-02 0 0
CUI: C1968633
Disease: Intimal thickening in the coronary arteries
Intimal thickening in the coronary arteries 		1 0 1 9.1E-02 0 0
CUI: C1968748
Disease: Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement
Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement 		1 0 1 9.1E-02 0 0
CUI: C2673257
Disease: EPILEPSY, PROGRESSIVE MYOCLONIC 3
EPILEPSY, PROGRESSIVE MYOCLONIC 3 		1 0 1 9.1E-02 0 0