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: C0221002
Disease: Hyperparathyroidism, Primary
Hyperparathyroidism, Primary
115 0 26 0.14 0 0
Hypocalciuric Hypercalcemia, Acquired
13 0 12 0.12 0 0
CUI: C0024106
Disease: Lumpy Skin Disease
Lumpy Skin Disease
12 0 11 0.11 0 0
CUI: C0857116
Disease: Gross obesity
Gross obesity
12 0 11 0.11 0 0
CUI: C1842402
Disease: TROPICAL CALCIFIC PANCREATITIS
TROPICAL CALCIFIC PANCREATITIS
24 0 12 0.11 0 0
POLYMICROGYRIA, BILATERAL FRONTOPARIETAL
15 0 11 0.11 0 0
CUI: C0342684
Disease: Ocular albinism, type I
Ocular albinism, type I
38 0 13 0.11 0 0
CUI: C0151846
Disease: Periosteal Disorder
Periosteal Disorder
80 0 17 0.11 0 0
CUI: C0162283
Disease: Nephrogenic Diabetes Insipidus
Nephrogenic Diabetes Insipidus
60 0 15 0.10 0 0
CUI: C1840311
Disease: Laryngeal cleft
Laryngeal cleft
72 0 16 0.10 0 0
CUI: C0220659
Disease: Acrodysostosis
Acrodysostosis
31 0 12 0.10 0 0
CUI: C0553665
Disease: Skin endocrine disorder
Skin endocrine disorder
34 0 12 1.0E-01 0 0
CUI: C1334386
Disease: Meningeal melanoma
Meningeal melanoma
23 0 11 1.0E-01 0 0
CUI: C0580174
Disease: Portal hypertensive gastropathy
Portal hypertensive gastropathy
24 0 11 9.9E-02 0 0
CUI: C0877008
Disease: Enzyme inhibition disorder
Enzyme inhibition disorder
171 0 24 9.8E-02 0 0
Hypocalciuric hypercalcemia, familial, type 1
46 0 12 9.1E-02 0 0
CUI: C0041948
Disease: Uremia
Uremia
110 0 17 8.9E-02 0 0
CUI: C0339510
Disease: Vitelliform Macular Dystrophy
Vitelliform Macular Dystrophy
74 0 14 8.9E-02 0 0
CUI: C0009917
Disease: Contracture
Contracture
111 0 17 8.9E-02 0 0
CUI: C1264039
Disease: von Willebrand Disease, Type 1
von Willebrand Disease, Type 1
39 0 11 8.7E-02 0 0
CUI: C0030521
Disease: Parathyroid Neoplasms
Parathyroid Neoplasms
104 0 16 8.6E-02 0 0
CUI: C0858600
Disease: Taste sweet
Taste sweet
41 0 11 8.6E-02 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome
68 0 13 8.5E-02 0 0
CUI: C0005818
Disease: Blood Platelet Disorders
Blood Platelet Disorders
59 0 12 8.3E-02 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 11 8.3E-02 0 0