Source: BEFREE ×
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: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 7.1E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 7.1E-02
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.5E-03 0 0
CUI: C0162283
Disease: Nephrogenic Diabetes Insipidus
Nephrogenic Diabetes Insipidus 		54 0 1 1.6E-03 0 0
CUI: C0342776
Disease: Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency 		51 0 1 1.6E-03 0 0
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses 		45 0 1 1.6E-03 0 0
CUI: C1857451
Disease: Acth-Independent Macronodular Adrenal Hyperplasia
Acth-Independent Macronodular Adrenal Hyperplasia 		44 0 1 1.6E-03 0 0
CUI: C0265202
Disease: Seckel syndrome
Seckel syndrome 		40 0 1 1.6E-03 0 0
CUI: C1264039
Disease: von Willebrand Disease, Type 1
von Willebrand Disease, Type 1 		39 0 1 1.6E-03 0 0
CUI: C0342684
Disease: Ocular albinism, type I
Ocular albinism, type I 		38 0 1 1.6E-03 0 0
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis 		37 0 1 1.6E-03 0 0
CUI: C3711376
Disease: Isodicentric Chromosome 15 Syndrome
Isodicentric Chromosome 15 Syndrome 		37 0 1 1.6E-03 0 0
CUI: C0020256
Disease: Congenital Hydrocephalus
Congenital Hydrocephalus 		34 0 1 1.7E-03 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		34 0 1 1.7E-03 0 0
CUI: C0878521
Disease: Beta thalassemia trait
Beta thalassemia trait 		34 0 1 1.7E-03 0 0
CUI: C0085292
Disease: Stiff-Person Syndrome
Stiff-Person Syndrome 		33 0 1 1.7E-03 0 0
CUI: C0154409
Disease: Recurrent major depressive episodes
Recurrent major depressive episodes 		32 0 1 1.7E-03 0 0
CUI: C0220659
Disease: Acrodysostosis
Acrodysostosis 		31 0 1 1.7E-03 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 1 1.7E-03 0 0
CUI: C1631597
Disease: VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) 		30 0 1 1.7E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		29 0 1 1.7E-03 0 0
CUI: C0085576
Disease: Iron-Refractory Iron Deficiency Anemia
Iron-Refractory Iron Deficiency Anemia 		29 0 1 1.7E-03 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2 		29 0 1 1.7E-03 0 0
CUI: C0026707
Disease: Mucopolysaccharidosis IV
Mucopolysaccharidosis IV 		28 0 1 1.7E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		28 0 1 1.7E-03 0 0