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: C0242350
Disease: Erectile dysfunction
Erectile dysfunction 		0 44 0 0 1 1.2E-02
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis 		0 29 0 0 1 1.4E-02
CUI: C1262106
Disease: Neuromuscular toxicity
Neuromuscular toxicity 		1 0 1 4.2E-02 0 0
CUI: C1863600
Disease: PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY (finding)
PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY (finding) 		1 0 1 4.2E-02 0 0
CUI: C3489787
Disease: Pituitary Hormone Deficiency, Combined, 3
Pituitary Hormone Deficiency, Combined, 3 		1 0 1 4.2E-02 0 0
CUI: C3541908
Disease: Sperm Motility Measurement
Sperm Motility Measurement 		1 0 1 4.2E-02 0 0
CUI: C3715155
Disease: AMYOTROPHIC LATERAL SCLEROSIS 19
AMYOTROPHIC LATERAL SCLEROSIS 19 		1 0 1 4.2E-02 0 0
CUI: C3810428
Disease: Hyperlaxity
Hyperlaxity 		1 0 1 4.2E-02 0 0
CUI: C4022967
Disease: Hypothalamic luteinizing hormone-releasing hormone deficiency
Hypothalamic luteinizing hormone-releasing hormone deficiency 		1 0 1 4.2E-02 0 0
CUI: C4727684
Disease: Metastatic Oral Cavity Squamous Cell Carcinoma
Metastatic Oral Cavity Squamous Cell Carcinoma 		1 0 1 4.2E-02 0 0
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		2 0 1 4.0E-02 0 0
CUI: C0850671
Disease: Non-diabetic hyperglycemia
Non-diabetic hyperglycemia 		2 0 1 4.0E-02 0 0
CUI: C1266049
Disease: Hyalinizing trabecular adenoma
Hyalinizing trabecular adenoma 		2 0 1 4.0E-02 0 0
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME 		2 0 1 4.0E-02 0 0
CUI: C1857775
Disease: Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 		2 0 1 4.0E-02 0 0
CUI: C4016905
Disease: HYPERBILIRUBINEMIA, ROTOR TYPE, DIGENIC
HYPERBILIRUBINEMIA, ROTOR TYPE, DIGENIC 		2 0 1 4.0E-02 0 0
CUI: C4022610
Disease: Excessive bleeding from superficial cuts
Excessive bleeding from superficial cuts 		2 0 1 4.0E-02 0 0
CUI: C0220991
Disease: Rotor Syndrome
Rotor Syndrome 		3 0 1 3.8E-02 0 0
CUI: C0398627
Disease: Inherited platelet disorder
Inherited platelet disorder 		3 0 1 3.8E-02 0 0
CUI: C1565885
Disease: Direct Hyperbilirubinemia, Neonatal
Direct Hyperbilirubinemia, Neonatal 		3 0 1 3.8E-02 0 0
CUI: C0546343
Disease: Mucosal erosion
Mucosal erosion 		4 0 1 3.7E-02 0 0
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		4 0 1 3.7E-02 0 0
CUI: C1446783
Disease: rings tracheal
rings tracheal 		4 0 1 3.7E-02 0 0
CUI: C1565886
Disease: Indirect Hyperbilirubinemia, Neonatal
Indirect Hyperbilirubinemia, Neonatal 		4 0 1 3.7E-02 0 0
CUI: C1864761
Disease: Thyroid Hormone Metabolism, Abnormal
Thyroid Hormone Metabolism, Abnormal 		4 5 1 3.7E-02 1 2.2E-02