Source: CURATED ×
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: C0020455
Disease: Hypergammaglobulinemia
Hypergammaglobulinemia 		1 0 1 0.20 0 0
CUI: C1622345
Disease: Meretoja syndrome
Meretoja syndrome 		1 0 1 0.20 0 0
CUI: C1628319
Disease: Lattice corneal dystrophy Type II
Lattice corneal dystrophy Type II 		1 0 1 0.20 0 0
CUI: C1855796
Disease: Hypoproteinemia, Hypercatabolic
Hypoproteinemia, Hypercatabolic 		1 0 1 0.20 0 0
CUI: C2751493
Disease: Cerebral Amyloid Angiopathy, Gsn-Related
Cerebral Amyloid Angiopathy, Gsn-Related 		1 0 1 0.20 0 0
CUI: C4016070
Disease: Fibrinogen dusart phenotype
Fibrinogen dusart phenotype 		1 0 1 0.20 0 0
CUI: C4087498
Disease: Familial LCAT deficiency
Familial LCAT deficiency 		1 0 1 0.20 0 0
CUI: C4302669
Disease: Autosomal dominant beta2-microglobulinic amyloidosis
Autosomal dominant beta2-microglobulinic amyloidosis 		1 0 1 0.20 0 0
CUI: C0079221
Disease: Determination of Death
Determination of Death 		2 0 1 0.17 0 0
CUI: C0154251
Disease: Lipid Metabolism Disorders
Lipid Metabolism Disorders 		2 0 1 0.17 0 0
CUI: C0342898
Disease: Apolipoprotein A-I deficiency
Apolipoprotein A-I deficiency 		2 0 1 0.17 0 0
CUI: C0376297
Disease: Cardiac Death
Cardiac Death 		2 0 1 0.17 0 0
CUI: C0936273
Disease: Familial Amyloid Polyneuropathy, Type IV
Familial Amyloid Polyneuropathy, Type IV 		2 0 1 0.17 0 0
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial 		2 0 1 0.17 0 0
CUI: C0272350
Disease: Dysfibrinogenemia, Congenital
Dysfibrinogenemia, Congenital 		3 0 1 0.14 0 0
CUI: C0740340
Disease: Amyloidosis, Familial
Amyloidosis, Familial 		3 0 1 0.14 0 0
CUI: C1848533
Disease: Ataxia with vitamin E deficiency
Ataxia with vitamin E deficiency 		3 0 1 0.14 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		4 0 1 0.12 0 0
CUI: C1858266
Disease: Bare Lymphocyte Syndrome, Type I
Bare Lymphocyte Syndrome, Type I 		4 0 1 0.12 0 0
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity 		4 0 1 0.12 0 0
CUI: C2584774
Disease: Congenital hypofibrinogenemia
Congenital hypofibrinogenemia 		4 0 1 0.12 0 0
CUI: C4317171
Disease: Adolescent Obesity
Adolescent Obesity 		4 0 1 0.12 0 0
CUI: C4521075
Disease: Childhood Overweight
Childhood Overweight 		4 0 1 0.12 0 0
CUI: C4553478
Disease: Infantile Obesity
Infantile Obesity 		4 0 1 0.12 0 0
CUI: C4704955
Disease: Infant Overweight
Infant Overweight 		4 0 1 0.12 0 0