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: C0428419
Disease: Triiodothyronine measurement
Triiodothyronine measurement 		6 12 3 0.11 6 0.12
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		42 83 5 8.2E-02 6 5.0E-02
CUI: C0441683
Disease: Hormone measurement
Hormone measurement 		51 134 5 7.1E-02 7 4.1E-02
CUI: C0015190
Disease: Euthyroid Sick Syndromes
Euthyroid Sick Syndromes 		9 0 2 6.5E-02 0 0
CUI: C0016065
Disease: Polyostotic fibrous dysplasia
Polyostotic fibrous dysplasia 		18 0 2 5.0E-02 0 0
CUI: C0342199
Disease: Iodine deficiency syndrome
Iodine deficiency syndrome 		22 0 2 4.5E-02 0 0
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: C0349218
Disease: Recurrent depressive disorder
Recurrent depressive disorder 		29 9 2 3.9E-02 1 2.0E-02
CUI: C1849718
Disease: POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE
POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE 		29 0 2 3.9E-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