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: C0233702
Disease: Algophobia
Algophobia
0 4 0 0 1 6.7E-02
CUI: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant
0 2 0 0 2 0.17
CUI: C0518964
Disease: BRONCHIAL ADENOCARCINOMA
BRONCHIAL ADENOCARCINOMA
0 1 0 0 1 8.3E-02
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy
73 0 1 2.7E-03 0 0
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly
70 0 1 2.7E-03 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
62 0 1 2.8E-03 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome
61 0 1 2.8E-03 0 0
CUI: C0014550
Disease: Myoclonic Epilepsy
Myoclonic Epilepsy
58 0 1 2.8E-03 0 0
CUI: C0020626
Disease: Hypoparathyroidism
Hypoparathyroidism
58 0 1 2.8E-03 0 0
CUI: C0683322
Disease: Mental impairment
Mental impairment
58 0 1 2.8E-03 0 0
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect
57 0 1 2.8E-03 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum
55 0 1 2.8E-03 0 0
CUI: C0038379
Disease: Strabismus
Strabismus
51 0 1 2.9E-03 0 0
CUI: C0233523
Disease: Antisocial behavior
Antisocial behavior
51 0 1 2.9E-03 0 0
CUI: C0038580
Disease: Substance Dependence
Substance Dependence
50 0 1 2.9E-03 0 0
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
50 0 1 2.9E-03 0 0
Acth-Independent Macronodular Adrenal Hyperplasia
44 0 1 2.9E-03 0 0
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
44 0 1 2.9E-03 0 0
CUI: C0017919
Disease: Glycogen Storage Disease
Glycogen Storage Disease
43 0 1 2.9E-03 0 0
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions
43 0 1 2.9E-03 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease
43 0 1 2.9E-03 0 0
CUI: C0457949
Disease: Chronic low back pain
Chronic low back pain
43 0 1 2.9E-03 0 0
CUI: C0004245
Disease: Atrioventricular Block
Atrioventricular Block
42 0 1 2.9E-03 0 0
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss
41 0 1 2.9E-03 0 0
Mitochondrial Respiratory Chain Deficiencies
40 0 1 2.9E-03 0 0