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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 3.5E-03
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 3 0 0 1 3.5E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 3.5E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.5E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 3.5E-03
CUI: C0814144
Disease: endocrine system cancer
endocrine system cancer 		0 1 0 0 1 3.5E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 3.5E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 3.5E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 3.5E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 3.5E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 3 1.1E-02
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		28 0 1 3.3E-04 0 0
CUI: C0751602
Disease: Hereditary Autosomal Dominant Spastic Paraplegia
Hereditary Autosomal Dominant Spastic Paraplegia 		22 0 1 3.3E-04 0 0
CUI: C3888090
Disease: Early onset torsion dystonia
Early onset torsion dystonia 		22 0 1 3.3E-04 0 0
CUI: C1843920
Disease: COENZYME Q10 DEFICIENCY
COENZYME Q10 DEFICIENCY 		21 0 1 3.3E-04 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		20 0 1 3.3E-04 0 0
CUI: C3468114
Disease: Juvenile amyotrophic lateral sclerosis
Juvenile amyotrophic lateral sclerosis 		20 0 1 3.3E-04 0 0
CUI: C4317123
Disease: Myoclonic Seizures
Myoclonic Seizures 		20 0 1 3.3E-04 0 0
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy 		18 0 1 3.3E-04 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 1 3.3E-04 0 0
CUI: C1854065
Disease: LATE-ONSET RETINAL DEGENERATION (disorder)
LATE-ONSET RETINAL DEGENERATION (disorder) 		17 0 1 3.3E-04 0 0
CUI: C0393556
Disease: Complicated hereditary spastic paraplegia
Complicated hereditary spastic paraplegia 		16 0 1 3.3E-04 0 0
CUI: C0752105
Disease: Parkinsonism, Juvenile
Parkinsonism, Juvenile 		16 0 1 3.3E-04 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		16 0 1 3.3E-04 0 0
CUI: C1859722
Disease: Arthrogryposis, renal dysfunction, and cholestasis 1
Arthrogryposis, renal dysfunction, and cholestasis 1 		16 0 1 3.3E-04 0 0