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: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 0 1 7.7E-02 0 0
CUI: C0268486
Disease: Hereditary hypertyrosinemia
Hereditary hypertyrosinemia 		1 0 1 7.7E-02 0 0
CUI: C0392178
Disease: Lipiduria
Lipiduria 		1 0 1 7.7E-02 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 7.7E-02 0 0
CUI: C1706559
Disease: Cornea verticillata
Cornea verticillata 		1 0 1 7.7E-02 0 0
CUI: C1833202
Disease: LCHAD DEFICIENCY WITH MATERNAL ACUTE FATTY LIVER OF PREGNANCY
LCHAD DEFICIENCY WITH MATERNAL ACUTE FATTY LIVER OF PREGNANCY 		1 0 1 7.7E-02 0 0
CUI: C1836460
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 		1 0 1 7.7E-02 0 0
CUI: C1848695
Disease: Episodic peripheral neuropathy
Episodic peripheral neuropathy 		1 0 1 7.7E-02 0 0
CUI: C1968739
Disease: Glycogen Storage Disease IIIA
Glycogen Storage Disease IIIA 		1 0 1 7.7E-02 0 0
CUI: C1968740
Disease: Glycogen Storage Disease IIIB
Glycogen Storage Disease IIIB 		1 0 1 7.7E-02 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 0 1 7.7E-02 0 0
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 0 1 7.7E-02 0 0
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 0 1 7.7E-02 0 0
CUI: C2936915
Disease: Amylo-1,6-glucosidase deficiency
Amylo-1,6-glucosidase deficiency 		1 0 1 7.7E-02 0 0
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 0 1 7.7E-02 0 0
CUI: C3266753
Disease: Severe left ventricular systolic dysfunction
Severe left ventricular systolic dysfunction 		1 0 1 7.7E-02 0 0
CUI: C3278154
Disease: GLUTARIC ACIDEMIA IIA
GLUTARIC ACIDEMIA IIA 		1 0 1 7.7E-02 0 0
CUI: C3278155
Disease: GLUTARIC ACIDEMIA IIB
GLUTARIC ACIDEMIA IIB 		1 0 1 7.7E-02 0 0
CUI: C3278156
Disease: GLUTARIC ACIDEMIA IIC
GLUTARIC ACIDEMIA IIC 		1 0 1 7.7E-02 0 0
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		1 0 1 7.7E-02 0 0
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