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: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8 		13 0 9 0.18 0 0
CUI: C0242292
Disease: McCune-Albright Syndrome
McCune-Albright Syndrome 		45 10 13 0.17 4 0.29
CUI: C1809471
Disease: Familial benign hypercalcemia
Familial benign hypercalcemia 		24 0 10 0.17 0 0
CUI: C0030521
Disease: Parathyroid Neoplasms
Parathyroid Neoplasms 		104 0 21 0.16 0 0
CUI: C0087169
Disease: Withdrawal Symptoms
Withdrawal Symptoms 		126 0 24 0.16 0 0
CUI: C0030517
Disease: Parathyroid Diseases
Parathyroid Diseases 		26 0 10 0.16 0 0
CUI: C0033806
Disease: Pseudohypoparathyroidism
Pseudohypoparathyroidism 		34 0 11 0.16 0 0
CUI: C0936282
Disease: Blastoma
Blastoma 		20 0 9 0.16 0 0
CUI: C4048195
Disease: Autosomal dominant hypocalcemia
Autosomal dominant hypocalcemia 		29 0 10 0.15 0 0
CUI: C0033117
Disease: Priapism
Priapism 		22 0 9 0.15 0 0
CUI: C0020175
Disease: Hunger
Hunger 		70 0 15 0.15 0 0
CUI: C1299624
Disease: Postural Orthostatic Tachycardia Syndrome
Postural Orthostatic Tachycardia Syndrome 		25 0 9 0.15 0 0
CUI: C3178766
Disease: Nociceptive Pain
Nociceptive Pain 		25 0 9 0.15 0 0
CUI: C0149911
Disease: Humoral hypercalcemia of malignancy (disorder)
Humoral hypercalcemia of malignancy (disorder) 		26 0 9 0.14 0 0
CUI: C1836672
Disease: Total Hypotrichosis, Mari type
Total Hypotrichosis, Mari type 		27 0 9 0.14 0 0
CUI: C0264657
Disease: Renal sclerosis with hypertension
Renal sclerosis with hypertension 		29 0 9 0.14 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 11 0.14 0 0
CUI: C0406810
Disease: Carney Complex
Carney Complex 		82 0 15 0.13 0 0
CUI: C0020071
Disease: Hereditary Sensory Autonomic Neuropathy, Type 1
Hereditary Sensory Autonomic Neuropathy, Type 1 		32 0 9 0.13 0 0
CUI: C0751569
Disease: Genitourinary Cancer
Genitourinary Cancer 		60 0 12 0.13 0 0
CUI: C0598428
Disease: genetic hypertension
genetic hypertension 		34 0 9 0.13 0 0
CUI: C0259779
Disease: Fibrous Dysplasia
Fibrous Dysplasia 		53 5 11 0.12 2 0.18
CUI: C4721452
Disease: Intestinal T-Cell Lymphoma
Intestinal T-Cell Lymphoma 		35 0 9 0.12 0 0
CUI: C0018834
Disease: Heartburn
Heartburn 		139 0 20 0.12 0 0
CUI: C0004775
Disease: Bartter Disease
Bartter Disease 		47 0 10 0.12 0 0