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: C0233397
Disease: Psychological symptom
Psychological symptom 		0 12 0 0 2 3.8E-02
CUI: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant 		0 2 0 0 2 4.7E-02
CUI: C0518964
Disease: BRONCHIAL ADENOCARCINOMA
BRONCHIAL ADENOCARCINOMA 		0 1 0 0 1 2.3E-02
CUI: C2931500
Disease: Microphthalmia and mental deficiency
Microphthalmia and mental deficiency 		0 6 0 0 1 2.1E-02
CUI: C4255043
Disease: Microphthalmos co-occurrent with congenital ocular coloboma
Microphthalmos co-occurrent with congenital ocular coloboma 		0 6 0 0 1 2.1E-02
CUI: C4524071
Disease: Philadelphia positive acute lymphocytic leukaemia
Philadelphia positive acute lymphocytic leukaemia 		0 1 0 0 1 2.3E-02
CUI: C4749271
Disease: Aleukemic mast cell leukemia
Aleukemic mast cell leukemia 		0 2 0 0 2 4.7E-02
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		81 0 1 1.8E-03 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		80 0 1 1.8E-03 0 0
CUI: C0700201
Disease: Dyssomnias
Dyssomnias 		75 0 1 1.8E-03 0 0
CUI: C0042693
Disease: Violence
Violence 		70 0 1 1.9E-03 0 0
CUI: C0947785
Disease: [D]Sleep disturbances (& [hypersomnia] or [insomnia])
[D]Sleep disturbances (& [hypersomnia] or [insomnia]) 		69 0 1 1.9E-03 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		62 0 1 1.9E-03 0 0
CUI: C0014550
Disease: Myoclonic Epilepsy
Myoclonic Epilepsy 		58 0 1 1.9E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		57 0 1 1.9E-03 0 0
CUI: C0424166
Disease: Social Anxiety
Social Anxiety 		57 0 1 1.9E-03 0 0
CUI: C1262211
Disease: Diarrhoea predominant irritable bowel syndrome
Diarrhoea predominant irritable bowel syndrome 		57 0 1 1.9E-03 0 0
CUI: C0342776
Disease: Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency 		51 0 1 1.9E-03 0 0
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 0 1 1.9E-03 0 0
CUI: C0342751
Disease: Generalized glycogen storage disease of infants
Generalized glycogen storage disease of infants 		50 0 1 1.9E-03 0 0
CUI: C0392164
Disease: Pulmonary Cystic Fibrosis
Pulmonary Cystic Fibrosis 		46 0 1 1.9E-03 0 0
CUI: C1609524
Disease: ADHF
ADHF 		46 0 1 1.9E-03 0 0
CUI: C0004775
Disease: Bartter Disease
Bartter Disease 		45 0 1 1.9E-03 0 0
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses 		45 0 1 1.9E-03 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		45 0 1 1.9E-03 0 0