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: C0020623
Disease: Hypolipoproteinemias
Hypolipoproteinemias 		1 0 1 4.0E-02 0 0
CUI: C0035326
Disease: Retinal vascular occlusion
Retinal vascular occlusion 		1 0 1 4.0E-02 0 0
CUI: C0149877
Disease: Hypoglycemic encephalopathy
Hypoglycemic encephalopathy 		1 0 1 4.0E-02 0 0
CUI: C0154298
Disease: Acute posthaemorrhagic anaemia
Acute posthaemorrhagic anaemia 		1 0 1 4.0E-02 0 0
CUI: C0234022
Disease: Anorgasmia
Anorgasmia 		1 0 1 4.0E-02 0 0
CUI: C0240709
Disease: Pericardial constriction
Pericardial constriction 		1 0 1 4.0E-02 0 0
CUI: C0268109
Disease: Chronic tophaceous gout
Chronic tophaceous gout 		1 0 1 4.0E-02 0 0
CUI: C0276044
Disease: Contagious bovine pleuropneumonia
Contagious bovine pleuropneumonia 		1 0 1 4.0E-02 0 0
CUI: C0279822
Disease: recurrent pheochromocytoma
recurrent pheochromocytoma 		1 0 1 4.0E-02 0 0
CUI: C0339495
Disease: Cilioretinal artery occlusion
Cilioretinal artery occlusion 		1 0 1 4.0E-02 0 0
CUI: C0585006
Disease: Deficiency of enoyl-CoA hydratase
Deficiency of enoyl-CoA hydratase 		1 0 1 4.0E-02 0 0
CUI: C0948824
Disease: Anemia due to blood loss
Anemia due to blood loss 		1 0 1 4.0E-02 0 0
CUI: C1456275
Disease: Mitochondrial metabolism disorder, unspecified
Mitochondrial metabolism disorder, unspecified 		1 0 1 4.0E-02 0 0
CUI: C1533628
Disease: Pseudo-Zellweger syndrome
Pseudo-Zellweger syndrome 		1 0 1 4.0E-02 0 0
CUI: C1720772
Disease: Hypoprebetalipoproteinemia
Hypoprebetalipoproteinemia 		1 0 1 4.0E-02 0 0
CUI: C1835362
Disease: Lp(A) Deficiency, Congenital
Lp(A) Deficiency, Congenital 		1 0 1 4.0E-02 0 0
CUI: C1841837
Disease: URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1
URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1 		1 0 1 4.0E-02 0 0
CUI: C1843983
Disease: Trapezoidal distal femoral condyles
Trapezoidal distal femoral condyles 		1 0 1 4.0E-02 0 0
CUI: C1843985
Disease: Shortening of the talar neck
Shortening of the talar neck 		1 0 1 4.0E-02 0 0
CUI: C1843986
Disease: Flattening of the talar dome
Flattening of the talar dome 		1 0 1 4.0E-02 0 0
CUI: C1859231
Disease: Hypoplastic olfactory lobes
Hypoplastic olfactory lobes 		1 0 1 4.0E-02 0 0
CUI: C1864948
Disease: Hyperinsulinemic Hypoglycemia, Familial, 4
Hyperinsulinemic Hypoglycemia, Familial, 4 		1 0 1 4.0E-02 0 0
CUI: C1866340
Disease: Peroxisome Biogenesis Disorder, Complementation Group 3
Peroxisome Biogenesis Disorder, Complementation Group 3 		1 0 1 4.0E-02 0 0
CUI: C1996989
Disease: Diarrhea due to drug
Diarrhea due to drug 		1 0 1 4.0E-02 0 0
CUI: C2673187
Disease: Erythrocytosis, Familial, 4
Erythrocytosis, Familial, 4 		1 0 1 4.0E-02 0 0