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: C0948825
Disease: Systremma
Systremma 		2 0 2 0.40 0 0
CUI: C0342162
Disease: Compensated hypothyroidism
Compensated hypothyroidism 		7 0 3 0.33 0 0
CUI: C0587044
Disease: Left ventricular thrombus
Left ventricular thrombus 		3 0 2 0.33 0 0
CUI: C1328551
Disease: Transfusion associated graft versus host disease
Transfusion associated graft versus host disease 		3 0 2 0.33 0 0
CUI: C3668940
Disease: Dmd-Associated Dilated Cardiomyopathy
Dmd-Associated Dilated Cardiomyopathy 		3 0 2 0.33 0 0
CUI: C0158983
Disease: Neonatal thyrotoxicosis
Neonatal thyrotoxicosis 		1 0 1 0.20 0 0
CUI: C0238185
Disease: Juvenile myxedema
Juvenile myxedema 		1 0 1 0.20 0 0
CUI: C0264733
Disease: Ventricular dilatation (disorder)
Ventricular dilatation (disorder) 		13 0 3 0.20 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 0.20 0 0
CUI: C0271149
Disease: Secondary angle-closure glaucoma
Secondary angle-closure glaucoma 		1 0 1 0.20 0 0
CUI: C0271152
Disease: Malignant glaucoma
Malignant glaucoma 		1 0 1 0.20 0 0
CUI: C0271814
Disease: Silent thyroiditis
Silent thyroiditis 		1 0 1 0.20 0 0
CUI: C0278861
Disease: Recurrent Thyroid Carcinoma
Recurrent Thyroid Carcinoma 		1 0 1 0.20 0 0
CUI: C0342114
Disease: Diffuse goiter
Diffuse goiter 		1 0 1 0.20 0 0
CUI: C0342134
Disease: T>3< thyrotoxicosis
T>3< thyrotoxicosis 		1 0 1 0.20 0 0
CUI: C0342136
Disease: Autonomous thyroid function
Autonomous thyroid function 		1 0 1 0.20 0 0
CUI: C0342194
Disease: Thyroid Dyshormonogenesis 3
Thyroid Dyshormonogenesis 3 		1 0 1 0.20 0 0
CUI: C0342377
Disease: Partial hypopituitarism
Partial hypopituitarism 		1 0 1 0.20 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 0.20 0 0
CUI: C0473565
Disease: Localized lipoatrophy
Localized lipoatrophy 		1 0 1 0.20 0 0
CUI: C0541403
Disease: Neuroendocrine disease or syndrome
Neuroendocrine disease or syndrome 		1 0 1 0.20 0 0
CUI: C0599725
Disease: colon growth
colon growth 		1 0 1 0.20 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 0.20 0 0
CUI: C0750731
Disease: Physical Appearance, Body
Physical Appearance, Body 		1 0 1 0.20 0 0
CUI: C0869147
Disease: Neonatal hyperthyroidism
Neonatal hyperthyroidism 		1 0 1 0.20 0 0