Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Familial Isolated Hyperparathyroidism
10 0 7 0.47 0 0
CUI: C0271846
Disease: Familial hyperparathyroidism
Familial hyperparathyroidism
7 0 5 0.36 0 0
CUI: C0745106
Disease: hyperparathyroid
hyperparathyroid
14 0 5 0.24 0 0
CUI: C0014132
Disease: Endocrine Gland Neoplasms
Endocrine Gland Neoplasms
15 0 5 0.23 0 0
CUI: C1809471
Disease: Familial benign hypercalcemia
Familial benign hypercalcemia
24 35 6 0.20 1 2.4E-02
Malignant tumor of parathyroid gland
13 0 4 0.19 0 0
CUI: C0030517
Disease: Parathyroid Diseases
Parathyroid Diseases
26 0 6 0.19 0 0
HYPERPARATHYROIDISM, NEONATAL SEVERE
14 0 4 0.18 0 0
CUI: C0278681
Disease: metastatic parathyroid cancer
metastatic parathyroid cancer
2 0 2 0.17 0 0
CUI: C0345406
Disease: Neonatal hyperparathyroidism
Neonatal hyperparathyroidism
2 0 2 0.17 0 0
CUI: C0865171
Disease: parathyroiditis
parathyroiditis
2 0 2 0.17 0 0
CUI: C2675664
Disease: PARATHYROID ADENOMA, SOMATIC
PARATHYROID ADENOMA, SOMATIC
2 0 2 0.17 0 0
CUI: C1403035
Disease: Subcutaneous lipoma
Subcutaneous lipoma
10 0 3 0.16 0 0
CUI: C0342634
Disease: Neonatal hypocalcemia
Neonatal hypocalcemia
3 0 2 0.15 0 0
Elevated circulating parathyroid hormone level
18 0 4 0.15 0 0
Increased circulating cortisol level
11 0 3 0.15 0 0
CUI: C0271844
Disease: Parathyroid hyperplasia
Parathyroid hyperplasia
37 0 6 0.14 0 0
Multiple Endocrine Neoplasia Type 2b
13 0 3 0.14 0 0
Multiple Endocrine Neoplasia, Type IV
13 0 3 0.14 0 0
CUI: C0006705
Disease: Calcium Metabolism Disorders
Calcium Metabolism Disorders
5 0 2 0.13 0 0
CUI: C0271858
Disease: Tertiary hyperparathyroidism
Tertiary hyperparathyroidism
5 0 2 0.13 0 0
CUI: C0475732
Disease: Hypercalcemia, Infantile
Hypercalcemia, Infantile
5 0 2 0.13 0 0
CUI: C1305409
Disease: Atypical adenoma
Atypical adenoma
5 0 2 0.13 0 0
CUI: C1704374
Disease: Carcinoma of Endocrine Gland
Carcinoma of Endocrine Gland
22 0 4 0.13 0 0
CUI: C3715128
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
5 0 2 0.13 0 0