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: C4048195
Disease: Autosomal dominant hypocalcemia
Autosomal dominant hypocalcemia 		29 0 21 0.21 0 0
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia 		94 13 31 0.20 2 7.7E-02
CUI: C0020438
Disease: Hypercalciuria
Hypercalciuria 		60 0 21 0.16 0 0
CUI: C0149911
Disease: Humoral hypercalcemia of malignancy (disorder)
Humoral hypercalcemia of malignancy (disorder) 		26 0 16 0.16 0 0
CUI: C0033806
Disease: Pseudohypoparathyroidism
Pseudohypoparathyroidism 		34 0 17 0.16 0 0
CUI: C0745730
Disease: Multiple lipomata
Multiple lipomata 		38 0 17 0.15 0 0
CUI: C1809471
Disease: Familial benign hypercalcemia
Familial benign hypercalcemia 		24 35 15 0.15 1 2.0E-02
CUI: C0234428
Disease: Disturbance of consciousness
Disturbance of consciousness 		35 0 16 0.14 0 0
CUI: C4021734
Disease: Abnormality of mitochondrial metabolism
Abnormality of mitochondrial metabolism 		21 0 14 0.14 0 0
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality 		23 0 14 0.14 0 0
CUI: C1836735
Disease: hypopigmented skin patch
hypopigmented skin patch 		123 0 26 0.14 0 0
CUI: C0039621
Disease: Tetany
Tetany 		24 0 14 0.14 0 0
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas 		33 0 15 0.14 0 0
CUI: C0030517
Disease: Parathyroid Diseases
Parathyroid Diseases 		26 0 14 0.13 0 0
CUI: C1857287
Disease: Stroke-like episode
Stroke-like episode 		27 0 14 0.13 0 0
CUI: C4520679
Disease: Abnormal macular morphology
Abnormal macular morphology 		30 0 14 0.13 0 0
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes 		31 0 14 0.13 0 0
CUI: C0149793
Disease: Amaurosis Fugax
Amaurosis Fugax 		49 0 16 0.13 0 0
CUI: C0151723
Disease: Hypomagnesemia
Hypomagnesemia 		58 0 17 0.13 0 0
CUI: C0020502
Disease: Hyperparathyroidism
Hyperparathyroidism 		111 0 22 0.12 0 0
CUI: C0040147
Disease: Thyroiditis
Thyroiditis 		104 0 21 0.12 0 0
CUI: C4025821
Disease: Anterior hypopituitarism
Anterior hypopituitarism 		48 0 15 0.12 0 0
CUI: C0342345
Disease: Hypoparathyroidism - autosomal dominant
Hypoparathyroidism - autosomal dominant 		12 44 11 0.12 1 1.7E-02
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 14 0.12 0 0
CUI: C1832615
Disease: HYPERPARATHYROIDISM, NEONATAL SEVERE
HYPERPARATHYROIDISM, NEONATAL SEVERE 		14 0 11 0.12 0 0