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: C3695006
Disease: GLYCOGEN STORAGE DISEASE, TYPE IIIb
GLYCOGEN STORAGE DISEASE, TYPE IIIb 		1 0 1 7.7E-02 0 0
CUI: C3695007
Disease: GLYCOGEN STORAGE DISEASE, TYPE IIIa
GLYCOGEN STORAGE DISEASE, TYPE IIIa 		1 0 1 7.7E-02 0 0
CUI: C3809443
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 12B (CARDIOMYOPATHIC TYPE), AUTOSOMAL RECESSIVE
MITOCHONDRIAL DNA DEPLETION SYNDROME 12B (CARDIOMYOPATHIC TYPE), AUTOSOMAL RECESSIVE 		1 0 1 7.7E-02 0 0
CUI: C4016438
Disease: GLUTARIC ACIDEMIA IIC, LATE-ONSET
GLUTARIC ACIDEMIA IIC, LATE-ONSET 		1 0 1 7.7E-02 0 0
CUI: C4310676
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT
MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT 		1 0 1 7.7E-02 0 0
CUI: C4321247
Disease: Mitochondrial DNA Depletion Syndrome 12
Mitochondrial DNA Depletion Syndrome 12 		1 0 1 7.7E-02 0 0
CUI: C0302280
Disease: Adrenogenital Syndrome
Adrenogenital Syndrome 		16 0 2 7.4E-02 0 0
CUI: C0027080
Disease: Myoglobinuria
Myoglobinuria 		17 0 2 7.1E-02 0 0
CUI: C0041323
Disease: Tuberculosis, Oral
Tuberculosis, Oral 		2 0 1 7.1E-02 0 0
CUI: C0149738
Disease: neurological pain
neurological pain 		2 0 1 7.1E-02 0 0
CUI: C0151861
Disease: Porphyruria
Porphyruria 		2 0 1 7.1E-02 0 0
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 0 1 7.1E-02 0 0
CUI: C0342886
Disease: Primary hypertriglyceridemia
Primary hypertriglyceridemia 		2 0 1 7.1E-02 0 0
CUI: C0751486
Disease: Reye-Like Syndrome
Reye-Like Syndrome 		2 0 1 7.1E-02 0 0
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		2 0 1 7.1E-02 0 0
CUI: C1291607
Disease: Deficiency of maleylacetoacetate isomerase
Deficiency of maleylacetoacetate isomerase 		2 0 1 7.1E-02 0 0
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		2 0 1 7.1E-02 0 0
CUI: C1968741
Disease: Glycogen Storage Disease IIIC
Glycogen Storage Disease IIIC 		2 0 1 7.1E-02 0 0
CUI: C1970820
Disease: Fabry Disease, Cardiac Variant
Fabry Disease, Cardiac Variant 		2 0 1 7.1E-02 0 0
CUI: C2936913
Disease: Porphyria, South African type
Porphyria, South African type 		2 0 1 7.1E-02 0 0
CUI: C4280773
Disease: Increased circulating free fatty acid level
Increased circulating free fatty acid level 		2 0 1 7.1E-02 0 0
CUI: C4551590
Disease: Familial renal hypouricemia
Familial renal hypouricemia 		2 0 1 7.1E-02 0 0
CUI: C0232726
Disease: Rectal tenesmus
Rectal tenesmus 		3 0 1 6.7E-02 0 0
CUI: C0234221
Disease: Acroparesthesia
Acroparesthesia 		3 0 1 6.7E-02 0 0
CUI: C0282507
Disease: Heat Stress Disorders
Heat Stress Disorders 		3 0 1 6.7E-02 0 0