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: C3875492
Disease: Hypocalciuric hypercalcemia
Hypocalciuric hypercalcemia 		5 0 2 0.13 0 0
CUI: C4552089
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME 		5 0 2 0.13 0 0
CUI: C4551632
Disease: Recurrent pancreatitis
Recurrent pancreatitis 		14 0 3 0.13 0 0
CUI: C1295677
Disease: Increased glucagon level
Increased glucagon level 		6 0 2 0.12 0 0
CUI: C1336751
Disease: Thyroid Hyalinizing Trabecular Adenoma
Thyroid Hyalinizing Trabecular Adenoma 		6 0 2 0.12 0 0
CUI: C3267007
Disease: Hypercalcitoninaemia
Hypercalcitoninaemia 		7 0 2 0.12 0 0
CUI: C0687150
Disease: Parathyroid Gland Adenocarcinoma
Parathyroid Gland Adenocarcinoma 		74 22 9 0.12 1 3.6E-02
CUI: C0342637
Disease: Hypocalciuric hypercalcemia, familial, type 1
Hypocalciuric hypercalcemia, familial, type 1 		46 58 6 0.12 1 1.6E-02
CUI: C0020503
Disease: Hyperparathyroidism, Secondary
Hyperparathyroidism, Secondary 		68 0 8 0.11 0 0
CUI: C1832648
Disease: Hypoparathyroidism familial isolated
Hypoparathyroidism familial isolated 		8 0 2 0.11 0 0
CUI: C1851705
Disease: Confetti-like hypopigmented macules
Confetti-like hypopigmented macules 		8 0 2 0.11 0 0
CUI: C4018860
Disease: Pituitary growth hormone cell adenoma
Pituitary growth hormone cell adenoma 		8 0 2 0.11 0 0
CUI: C4023068
Disease: Increased urinary cortisol level
Increased urinary cortisol level 		8 0 2 0.11 0 0
CUI: C0206640
Disease: Ossifying Fibroma
Ossifying Fibroma 		19 0 3 0.11 0 0
CUI: C0280787
Disease: Adult Anaplastic Ependymoma
Adult Anaplastic Ependymoma 		9 0 2 0.11 0 0
CUI: C4086151
Disease: Childhood Anaplastic Ependymoma
Childhood Anaplastic Ependymoma 		9 0 2 0.11 0 0
CUI: C0027662
Disease: Multiple Endocrine Neoplasia
Multiple Endocrine Neoplasia 		65 0 7 1.0E-01 0 0
CUI: C0151714
Disease: Hypermagnesemia
Hypermagnesemia 		10 0 2 1.0E-01 0 0
CUI: C0393590
Disease: Fahr's syndrome (disorder)
Fahr's syndrome (disorder) 		10 0 2 1.0E-01 0 0
CUI: C1864954
Disease: Fasting hyperinsulinemia
Fasting hyperinsulinemia 		10 0 2 1.0E-01 0 0
CUI: C1336750
Disease: Thyroid Gland Oncocytic Adenoma
Thyroid Gland Oncocytic Adenoma 		11 0 2 9.5E-02 0 0
CUI: C1865292
Disease: Nonketotic hypoglycemia
Nonketotic hypoglycemia 		11 0 2 9.5E-02 0 0
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		12 0 2 9.1E-02 0 0
CUI: C0342345
Disease: Hypoparathyroidism - autosomal dominant
Hypoparathyroidism - autosomal dominant 		12 44 2 9.1E-02 1 2.0E-02
CUI: C0026141
Disease: Milk-Alkali Syndrome
Milk-Alkali Syndrome 		13 0 2 8.7E-02 0 0