Source: ALL
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: C0002894
Disease: Refractory anaemia with excess blasts
Refractory anaemia with excess blasts 		0 2 0 0 1 2.1E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 1.9E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.2E-02
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		0 35 0 0 2 2.5E-02
CUI: C0151311
Disease: Cranial nerve palsies
Cranial nerve palsies 		0 1 0 0 1 2.2E-02
CUI: C0242073
Disease: Pulmonary congestion
Pulmonary congestion 		0 1 0 0 1 2.2E-02
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney 		0 8 0 0 1 1.9E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 3 6.2E-02
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome 		0 144 0 0 2 1.1E-02
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome 		0 2 0 0 1 2.1E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 1 2.1E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 2.1E-02
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		0 21 0 0 3 4.7E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 13 0 0 1 1.7E-02
CUI: C2676507
Disease: Inflammatory Bowel Disease 21
Inflammatory Bowel Disease 21 		0 1 0 0 1 2.2E-02
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft 		0 2 0 0 2 4.3E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 2.1E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.2E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 3 6.5E-02
CUI: C0000880
Disease: Acanthamoeba Keratitis
Acanthamoeba Keratitis 		22 0 1 9.3E-03 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 1 7.6E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 1 9.5E-03 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 1.1E-02 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 1.1E-02 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 4 1 1.1E-02 1 2.0E-02