Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Congenital hypothyroidism without goiter
1 0 1 1.00 0 0
CUI: C0342154
Disease: Congenital atrophy of thyroid
Congenital atrophy of thyroid
1 0 1 1.00 0 0
HYPOTHYROIDISM, CENTRAL, AND TESTICULAR ENLARGEMENT
1 0 1 1.00 0 0
CUI: C1578691
Disease: Myxedema, Congenital
Myxedema, Congenital
4 0 1 0.25 0 0
CUI: C1836264
Disease: Congenital bilateral ptosis
Congenital bilateral ptosis
4 0 1 0.25 0 0
CUI: C4302200
Disease: Congenital central hypothyroidism
Congenital central hypothyroidism
8 0 1 0.12 0 0
CUI: C0749420
Disease: Thyroid Agenesis
Thyroid Agenesis
11 0 1 9.1E-02 0 0
CUI: C0017547
Disease: Gigantism
Gigantism
16 0 1 6.2E-02 0 0
CUI: C0039584
Disease: Testicular Diseases
Testicular Diseases
16 0 1 6.2E-02 0 0
Constitutional delay of growth and puberty
16 0 1 6.2E-02 0 0
CUI: C1263023
Disease: Macroorchidism
Macroorchidism
16 0 1 6.2E-02 0 0
CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder)
22 0 1 4.5E-02 0 0
CUI: C0342200
Disease: Endemic Cretinism
Endemic Cretinism
26 0 1 3.8E-02 0 0
CUI: C0497406
Disease: Overweight
Overweight
27 0 1 3.7E-02 0 0
CUI: C0271801
Disease: Central hypothyroidism
Central hypothyroidism
35 0 1 2.9E-02 0 0
Columnar Cell Hyperplasia of the Breast
38 0 1 2.6E-02 0 0
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism
47 0 1 2.1E-02 0 0
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism
69 0 1 1.4E-02 0 0
CUI: C0033575
Disease: Prostatic Diseases
Prostatic Diseases
72 0 1 1.4E-02 0 0
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism
94 0 1 1.1E-02 0 0
CUI: C0019208
Disease: Hepatoma, Novikoff
Hepatoma, Novikoff
125 0 1 8.0E-03 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly
138 0 1 7.2E-03 0 0
CUI: C0007130
Disease: Mucinous Adenocarcinoma
Mucinous Adenocarcinoma
159 0 1 6.3E-03 0 0
CUI: C0151546
Disease: Oral Cavity Carcinoma
Oral Cavity Carcinoma
167 0 1 6.0E-03 0 0
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency
168 0 1 6.0E-03 0 0