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: C4551984
Disease: Arthrogryposis with renal dysfunction and cholestasis syndrome
Arthrogryposis with renal dysfunction and cholestasis syndrome 		12 0 1 2.7E-04 0 0
CUI: C0332915
Disease: Congenital failure of fusion
Congenital failure of fusion 		11 0 1 2.7E-04 0 0
CUI: C0342191
Disease: Familial dyshormonogenetic goiter
Familial dyshormonogenetic goiter 		11 0 1 2.7E-04 0 0
CUI: C0549225
Disease: Myasthenic Syndrome
Myasthenic Syndrome 		11 0 1 2.7E-04 0 0
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness 		11 0 1 2.7E-04 0 0
CUI: C1868596
Disease: Atypical Parkinson Disease
Atypical Parkinson Disease 		11 0 1 2.7E-04 0 0
CUI: C1955603
Disease: Deaf-Blind Disorders
Deaf-Blind Disorders 		11 0 1 2.7E-04 0 0
CUI: C0149841
Disease: Benign recurrent intrahepatic cholestasis
Benign recurrent intrahepatic cholestasis 		10 0 1 2.7E-04 0 0
CUI: C0270707
Disease: Kluver-Bucy Syndrome
Kluver-Bucy Syndrome 		10 0 1 2.7E-04 0 0
CUI: C0271091
Disease: Retinoschisis, Juvenile, X-Linked
Retinoschisis, Juvenile, X-Linked 		10 0 1 2.7E-04 0 0
CUI: C0342778
Disease: Ubiquinone dehydrogenase deficiency
Ubiquinone dehydrogenase deficiency 		10 0 1 2.7E-04 0 0
CUI: C0349653
Disease: Congenital disorder of glycosylation type 1A
Congenital disorder of glycosylation type 1A 		10 0 1 2.7E-04 0 0
CUI: C0432217
Disease: Wolcott-Rallison syndrome
Wolcott-Rallison syndrome 		10 0 1 2.7E-04 0 0
CUI: C0543918
Disease: SCHIZOPHRENIA 10
SCHIZOPHRENIA 10 		10 0 1 2.7E-04 0 0
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		10 0 1 2.7E-04 0 0
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome 		10 0 1 2.7E-04 0 0
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder) 		9 0 1 2.7E-04 0 0
CUI: C0271583
Disease: ACTH Deficiency, Isolated
ACTH Deficiency, Isolated 		9 0 1 2.7E-04 0 0
CUI: C0342471
Disease: 3 beta-Hydroxysteroid dehydrogenase deficiency
3 beta-Hydroxysteroid dehydrogenase deficiency 		9 0 1 2.7E-04 0 0
CUI: C0432185
Disease: Aplasia of muscle
Aplasia of muscle 		9 0 1 2.7E-04 0 0
CUI: C0752202
Disease: Childhood Onset Dystonias
Childhood Onset Dystonias 		9 0 1 2.7E-04 0 0
CUI: C0752207
Disease: Familial Dystonia
Familial Dystonia 		9 0 1 2.7E-04 0 0
CUI: C1848200
Disease: SUBCORTICAL BAND HETEROTOPIA, X-LINKED
SUBCORTICAL BAND HETEROTOPIA, X-LINKED 		9 0 1 2.7E-04 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 1 2.7E-04 0 0
CUI: C1858479
Disease: Spastic paraplegia 11, autosomal recessive
Spastic paraplegia 11, autosomal recessive 		9 0 1 2.7E-04 0 0