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: C0020550
Disease: Hyperthyroidism
Hyperthyroidism 		279 27 24 6.9E-02 1 1.4E-02
CUI: C0033806
Disease: Pseudohypoparathyroidism
Pseudohypoparathyroidism 		34 0 8 6.7E-02 0 0
CUI: C0041408
Disease: Turner Syndrome
Turner Syndrome 		162 0 16 6.7E-02 0 0
CUI: C1845847
Disease: Coarse facial features
Coarse facial features 		194 0 18 6.7E-02 0 0
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases 		230 0 20 6.6E-02 0 0
CUI: C1848805
Disease: Thyroid Dyshormonogenesis 1
Thyroid Dyshormonogenesis 1 		6 7 6 6.4E-02 1 1.9E-02
CUI: C3715197
Disease: Primary congenital hypothyroidism
Primary congenital hypothyroidism 		6 0 6 6.4E-02 0 0
CUI: C4023574
Disease: Abnormality of circulating adrenocorticotropin level
Abnormality of circulating adrenocorticotropin level 		6 0 6 6.4E-02 0 0
CUI: C0022346
Disease: Icterus
Icterus 		241 0 20 6.3E-02 0 0
CUI: C4302200
Disease: Congenital central hypothyroidism
Congenital central hypothyroidism 		8 0 6 6.2E-02 0 0
CUI: C0271791
Disease: Severe hypothyroidism
Severe hypothyroidism 		9 0 6 6.2E-02 0 0
CUI: C4023190
Disease: Thyroid hemiagenesis
Thyroid hemiagenesis 		9 0 6 6.2E-02 0 0
CUI: C0040137
Disease: Thyroid Nodule
Thyroid Nodule 		150 0 14 6.1E-02 0 0
CUI: C4049650
Disease: Familial Glucocorticoid Deficiency Type 1
Familial Glucocorticoid Deficiency Type 1 		12 0 6 6.0E-02 0 0
CUI: C0271561
Disease: Somatotropin deficiency
Somatotropin deficiency 		154 0 14 6.0E-02 0 0
CUI: C0700502
Disease: Acquired hypothyroidism
Acquired hypothyroidism 		13 2 6 5.9E-02 1 2.0E-02
CUI: C0001206
Disease: Acromegaly
Acromegaly 		138 0 13 5.9E-02 0 0
CUI: C0034013
Disease: Precocious Puberty
Precocious Puberty 		139 0 13 5.9E-02 0 0
CUI: C0342208
Disease: Multinodular goiter
Multinodular goiter 		51 6 8 5.8E-02 1 1.9E-02
CUI: C0271713
Disease: Ketotic hypoglycemia
Ketotic hypoglycemia 		15 0 6 5.8E-02 0 0
CUI: C0405580
Disease: Adrenal cortical hypofunction
Adrenal cortical hypofunction 		52 0 8 5.8E-02 0 0
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos 		235 0 18 5.8E-02 0 0
CUI: C0342409
Disease: Hypophysitis
Hypophysitis 		19 0 6 5.6E-02 0 0
CUI: C0221406
Disease: Pituitary-dependent Cushing's disease
Pituitary-dependent Cushing's disease 		115 0 11 5.6E-02 0 0
CUI: C0009806
Disease: Constipation
Constipation 		424 0 27 5.5E-02 0 0