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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 1 0 0 1 0.14
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 0.14
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 0.14
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 2 0.20
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		0 2 0 0 2 0.29
CUI: C0518964
Disease: BRONCHIAL ADENOCARCINOMA
BRONCHIAL ADENOCARCINOMA 		0 1 0 0 1 0.14
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft 		0 2 0 0 1 0.12
CUI: C3272525
Disease: Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma
Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma 		0 2 0 0 2 0.29
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 0.14
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 0.11
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1 		0 7 0 0 1 7.7E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 0.14
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 0.12
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 6.7E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 0.25
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 1 6.5E-03 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		30 0 1 7.3E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory 		12 0 1 8.4E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 8.5E-03 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis 		9 0 1 8.6E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 8.7E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		8 4 1 8.7E-03 2 0.22
CUI: C0001614
Disease: Adrenal Cortex Diseases
Adrenal Cortex Diseases 		13 0 1 8.3E-03 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia 		74 0 1 5.5E-03 0 0
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic 		16 0 1 8.1E-03 0 0