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: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0 5 0 0 3 0.23
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 1 0 0 1 9.1E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 9.1E-02
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		0 23 0 0 2 6.2E-02
CUI: C0151311
Disease: Cranial nerve palsies
Cranial nerve palsies 		0 1 0 0 1 9.1E-02
CUI: C0242073
Disease: Pulmonary congestion
Pulmonary congestion 		0 1 0 0 1 9.1E-02
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 9.1E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 3 0.23
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome 		0 17 0 0 2 7.7E-02
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		0 3 0 0 3 0.27
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 12 0 0 1 4.5E-02
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft 		0 2 0 0 1 8.3E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 7.7E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 9.1E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 2 0.11
CUI: C4725671
Disease: High-Risk Neuroblastoma
High-Risk Neuroblastoma 		0 4 0 0 1 7.1E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 0.17
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms 		13 0 1 2.3E-02 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		74 0 1 9.6E-03 0 0
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		79 0 1 9.2E-03 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 2.6E-02 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		8 4 1 2.6E-02 1 7.1E-02
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic 		16 0 1 2.2E-02 0 0
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms 		23 0 1 1.9E-02 0 0
CUI: C0001787
Disease: Osteoporosis, Age-Related
Osteoporosis, Age-Related 		31 0 1 1.6E-02 0 0