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: C3494506
Disease: Pseudohypoparathyroidism, Type Ia
Pseudohypoparathyroidism, Type Ia
30 0 20 0.45 0 0
Albright's hereditary osteodystrophy
22 0 16 0.40 0 0
CUI: C0033835
Disease: Pseudopseudohypoparathyroidism
Pseudopseudohypoparathyroidism
14 0 13 0.37 0 0
Primary pigmented nodular adrenocortical disease
22 0 13 0.30 0 0
CUI: C0220659
Disease: Acrodysostosis
Acrodysostosis
31 6 15 0.30 4 0.67
Humoral hypercalcemia of malignancy (disorder)
26 0 13 0.28 0 0
CUI: C0241893
Disease: Tick fever
Tick fever
9 0 9 0.26 0 0
CUI: C0276849
Disease: Infection by Babesia bovis
Infection by Babesia bovis
9 0 9 0.26 0 0
CUI: C1274989
Disease: Retinoid dermatitis
Retinoid dermatitis
9 0 9 0.26 0 0
CUI: C1809471
Disease: Familial benign hypercalcemia
Familial benign hypercalcemia
24 0 12 0.26 0 0
CUI: C0157743
Disease: Vibratory urticaria
Vibratory urticaria
10 0 9 0.26 0 0
CUI: C0597854
Disease: renin induced hypertension
renin induced hypertension
11 0 9 0.25 0 0
CUI: C1864100
Disease: PSEUDOHYPOPARATHYROIDISM, TYPE IB
PSEUDOHYPOPARATHYROIDISM, TYPE IB
13 0 9 0.24 0 0
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8
13 0 9 0.24 0 0
CUI: C0242292
Disease: McCune-Albright Syndrome
McCune-Albright Syndrome
45 0 15 0.23 0 0
Nephrogenic Syndrome of Inappropriate Antidiuresis
14 0 9 0.23 0 0
CUI: C0342494
Disease: Adrenocortical hyperplasia
Adrenocortical hyperplasia
25 0 11 0.23 0 0
Primary Pigmented Nodular Adrenal Dysplasia
31 0 12 0.23 0 0
CUI: C0259779
Disease: Fibrous Dysplasia
Fibrous Dysplasia
53 0 16 0.23 0 0
CUI: C1535964
Disease: Cholestatic pruritus
Cholestatic pruritus
15 0 9 0.23 0 0
CUI: C0030517
Disease: Parathyroid Diseases
Parathyroid Diseases
26 0 11 0.22 0 0
CUI: C4048195
Disease: Autosomal dominant hypocalcemia
Autosomal dominant hypocalcemia
29 0 11 0.21 0 0
CUI: C0936282
Disease: Blastoma
Blastoma
20 0 9 0.20 0 0
CUI: C2932715
Disease: Pseudohypoparathyroidism Type 1B
Pseudohypoparathyroidism Type 1B
8 0 7 0.20 0 0
CUI: C0598428
Disease: genetic hypertension
genetic hypertension
34 0 11 0.19 0 0