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: C0240952
Disease: Dysarthria, Scanning
Dysarthria, Scanning 		2 0 2 1.00 0 0
CUI: C0454598
Disease: Dysarthria, Mixed
Dysarthria, Mixed 		2 0 2 1.00 0 0
CUI: C1563666
Disease: Dysarthria, Guttural
Dysarthria, Guttural 		2 0 2 1.00 0 0
CUI: C0280214
Disease: stage, nasopharyngeal cancer
stage, nasopharyngeal cancer 		1 0 1 0.50 0 0
CUI: C1850363
Disease: Niemann-Pick Disease, Nova Scotian Type
Niemann-Pick Disease, Nova Scotian Type 		1 0 1 0.50 0 0
CUI: C1997262
Disease: Hypothyroidism in pregnancy
Hypothyroidism in pregnancy 		1 0 1 0.50 0 0
CUI: C2231324
Disease: Brucellosis, Pulmonary
Brucellosis, Pulmonary 		1 0 1 0.50 0 0
CUI: C3280094
Disease: PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3 		1 0 1 0.50 0 0
CUI: C4017105
Disease: NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM
NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM 		1 0 1 0.50 0 0
CUI: C4017106
Disease: NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM
NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM 		1 0 1 0.50 0 0
CUI: C4024947
Disease: Symmetric lesions of the basal ganglia
Symmetric lesions of the basal ganglia 		1 0 1 0.50 0 0
CUI: C4310808
Disease: STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 1
STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 1 		1 0 1 0.50 0 0
CUI: C0268247
Disease: Niemann-Pick Disease, Type D
Niemann-Pick Disease, Type D 		2 0 1 0.33 0 0
CUI: C1836694
Disease: Striatal Degeneration, Autosomal Dominant
Striatal Degeneration, Autosomal Dominant 		2 0 1 0.33 0 0
CUI: C1843373
Disease: Foam cells in visceral organs and CNS
Foam cells in visceral organs and CNS 		2 0 1 0.33 0 0
CUI: C2713319
Disease: Arylsulfatase A Deficiency
Arylsulfatase A Deficiency 		2 0 1 0.33 0 0
CUI: C0264542
Disease: Adhesion of pleura
Adhesion of pleura 		3 0 1 0.25 0 0
CUI: C1881236
Disease: Interstitial Disease
Interstitial Disease 		3 0 1 0.25 0 0
CUI: C4025017
Disease: Fatal liver failure in infancy
Fatal liver failure in infancy 		3 0 1 0.25 0 0
CUI: C1968851
Disease: Pigmented micronodular adrenocortical disease
Pigmented micronodular adrenocortical disease 		4 0 1 0.20 0 0
CUI: C0036489
Disease: Sea-Blue Histiocyte Syndrome
Sea-Blue Histiocyte Syndrome 		5 0 1 0.17 0 0
CUI: C0231519
Disease: Gegenhalten
Gegenhalten 		5 0 1 0.17 0 0
CUI: C0233608
Disease: Catatonic Rigidity
Catatonic Rigidity 		5 0 1 0.17 0 0
CUI: C0239325
Disease: Extensor Rigidity
Extensor Rigidity 		5 0 1 0.17 0 0
CUI: C0277821
Disease: Extrapyramidal Rigidity
Extrapyramidal Rigidity 		5 0 1 0.17 0 0