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: C0087169
Disease: Withdrawal Symptoms
Withdrawal Symptoms
126 0 23 0.14 0 0
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8
13 0 9 0.14 0 0
CUI: C0033117
Disease: Priapism
Priapism
22 0 10 0.14 0 0
CUI: C1809471
Disease: Familial benign hypercalcemia
Familial benign hypercalcemia
24 0 10 0.14 0 0
Postural Orthostatic Tachycardia Syndrome
25 0 10 0.13 0 0
CUI: C0030517
Disease: Parathyroid Diseases
Parathyroid Diseases
26 0 10 0.13 0 0
Humoral hypercalcemia of malignancy (disorder)
26 0 10 0.13 0 0
CUI: C0936282
Disease: Blastoma
Blastoma
20 0 9 0.13 0 0
CUI: C4048195
Disease: Autosomal dominant hypocalcemia
Autosomal dominant hypocalcemia
29 0 10 0.13 0 0
Primary pigmented nodular adrenocortical disease
22 0 9 0.12 0 0
CUI: C0005818
Disease: Blood Platelet Disorders
Blood Platelet Disorders
59 0 13 0.12 0 0
CUI: C1285162
Disease: Degenerative disorder
Degenerative disorder
160 0 24 0.12 0 0
CUI: C0033806
Disease: Pseudohypoparathyroidism
Pseudohypoparathyroidism
34 0 10 0.12 0 0
CUI: C0598428
Disease: genetic hypertension
genetic hypertension
34 0 10 0.12 0 0
CUI: C0342494
Disease: Adrenocortical hyperplasia
Adrenocortical hyperplasia
25 0 9 0.12 0 0
CUI: C3178766
Disease: Nociceptive Pain
Nociceptive Pain
25 0 9 0.12 0 0
CUI: C0032617
Disease: Polyuria
Polyuria
73 0 14 0.12 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 11 0.12 0 0
CUI: C1836672
Disease: Total Hypotrichosis, Mari type
Total Hypotrichosis, Mari type
27 0 9 0.12 0 0
CUI: C0264657
Disease: Renal sclerosis with hypertension
Renal sclerosis with hypertension
29 0 9 0.11 0 0
CUI: C0018834
Disease: Heartburn
Heartburn
139 0 20 0.11 0 0
CUI: C0751569
Disease: Genitourinary Cancer
Genitourinary Cancer
60 0 12 0.11 0 0
Primary Pigmented Nodular Adrenal Dysplasia
31 0 9 0.11 0 0
Hereditary Sensory Autonomic Neuropathy, Type 1
32 0 9 0.11 0 0
CUI: C0392164
Disease: Pulmonary Cystic Fibrosis
Pulmonary Cystic Fibrosis
53 0 11 0.11 0 0