Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Mixed Somatotroph and Lactotroph Adenoma
2 0 2 0.13 0 0
CUI: C0014008
Disease: Empty Sella Syndrome
Empty Sella Syndrome
3 0 2 0.12 0 0
CUI: C0271449
Disease: Exudative otitis media
Exudative otitis media
3 0 2 0.12 0 0
CUI: C0858734
Disease: Insulin hypoglycemia
Insulin hypoglycemia
5 0 2 0.11 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia
6 0 2 0.11 0 0
CUI: C0344453
Disease: Macroprolactinoma
Macroprolactinoma
7 0 2 1.0E-01 0 0
CUI: C0684516
Disease: Benign bone neoplasm
Benign bone neoplasm
8 0 2 9.5E-02 0 0
CUI: C0851135
Disease: In situ cancer
In situ cancer
8 0 2 9.5E-02 0 0
CUI: C1709286
Disease: Null Cell Pituitary Gland Adenoma
Null Cell Pituitary Gland Adenoma
9 0 2 9.1E-02 0 0
Follicle stimulating hormone deficiency
10 0 2 8.7E-02 0 0
CUI: C0264766
Disease: Rheumatic mitral stenosis
Rheumatic mitral stenosis
12 0 2 8.0E-02 0 0
CUI: C0751230
Disease: Hypothalamic Dysfunction Syndromes
Hypothalamic Dysfunction Syndromes
12 0 2 8.0E-02 0 0
CUI: C0700502
Disease: Acquired hypothyroidism
Acquired hypothyroidism
13 0 2 7.7E-02 0 0
CUI: C4316995
Disease: Primary Hypothyroidism
Primary Hypothyroidism
13 0 2 7.7E-02 0 0
CUI: C0149825
Disease: Hypertrophy of adenoids
Hypertrophy of adenoids
14 0 2 7.4E-02 0 0
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes
14 0 2 7.4E-02 0 0
CUI: C0406500
Disease: Lipodermatosclerosis
Lipodermatosclerosis
14 0 2 7.4E-02 0 0
CUI: C3696962
Disease: Coronary microvascular dysfunction
Coronary microvascular dysfunction
14 0 2 7.4E-02 0 0
CUI: C4704874
Disease: Mammary Carcinoma, Human
Mammary Carcinoma, Human
29 0 3 7.3E-02 0 0
CUI: C0280317
Disease: Squamous cell carcinoma of tonsil
Squamous cell carcinoma of tonsil
30 0 3 7.1E-02 0 0
CUI: C1096666
Disease: Thyroid cancer metastatic
Thyroid cancer metastatic
15 0 2 7.1E-02 0 0
FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, OF SORSBY
15 0 2 7.1E-02 0 0
CUI: C0017547
Disease: Gigantism
Gigantism
16 0 2 6.9E-02 0 0
CUI: C1328407
Disease: Hip Dysplasia
Hip Dysplasia
16 0 2 6.9E-02 0 0
PITUITARY ADENOMA, FAMILIAL ISOLATED (disorder)
16 0 2 6.9E-02 0 0