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: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 3 0 0 1 9.0E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 9.2E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 9.2E-03
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 1 9.1E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 9.1E-03
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		57 0 1 7.9E-04 0 0
CUI: C0206157
Disease: Myopathies, Nemaline
Myopathies, Nemaline 		34 0 1 8.0E-04 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		34 0 1 8.0E-04 0 0
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome 		31 0 1 8.0E-04 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 1 8.0E-04 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		30 0 1 8.0E-04 0 0
CUI: C0751435
Disease: Hyperphenylalaninaemia
Hyperphenylalaninaemia 		30 0 1 8.0E-04 0 0
CUI: C0268583
Disease: Methylmalonic acidemia
Methylmalonic acidemia 		28 0 1 8.1E-04 0 0
CUI: C0871215
Disease: Reading Disabilities
Reading Disabilities 		28 0 1 8.1E-04 0 0
CUI: C0043207
Disease: Wolfram Syndrome
Wolfram Syndrome 		25 0 1 8.1E-04 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		25 0 1 8.1E-04 0 0
CUI: C0023794
Disease: Lipoidosis
Lipoidosis 		23 0 1 8.1E-04 0 0
CUI: C0078917
Disease: Albinism, Ocular
Albinism, Ocular 		23 0 1 8.1E-04 0 0
CUI: C0023092
Disease: Lassa Fever
Lassa Fever 		22 0 1 8.1E-04 0 0
CUI: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency 		22 0 1 8.1E-04 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		22 0 1 8.1E-04 0 0
CUI: C1848641
Disease: Profound sensorineural hearing loss
Profound sensorineural hearing loss 		22 0 1 8.1E-04 0 0
CUI: C3826457
Disease: Diabetes in children
Diabetes in children 		22 0 1 8.1E-04 0 0
CUI: C3890602
Disease: Bodily Pain
Bodily Pain 		22 4 1 8.1E-04 1 8.9E-03
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent 		21 0 1 8.1E-04 0 0