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: C0749420
Disease: Thyroid Agenesis
Thyroid Agenesis
11 0 5 0.36 0 0
CUI: C0342196
Disease: Thyroid Dyshormonogenesis 5
Thyroid Dyshormonogenesis 5
4 0 3 0.33 0 0
CUI: C0349476
Disease: Congenital goiter
Congenital goiter
7 0 3 0.25 0 0
Endometrioid adenocarcinoma metastatic
2 0 2 0.25 0 0
Granular cell tumor of the sellar region
2 0 2 0.25 0 0
Granular Cell Tumor of the Neurohypophysis
2 0 2 0.25 0 0
Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress
7 0 3 0.25 0 0
Malignant epithelial neoplasm of thyroid
2 0 2 0.25 0 0
CUI: C0155964
Disease: Atrophy of tongue papillae
Atrophy of tongue papillae
3 0 2 0.22 0 0
CUI: C0748616
Disease: Sellar Region Neoplasm
Sellar Region Neoplasm
3 0 2 0.22 0 0
Thyroid Gland Carcinoma Showing Thymus-Like Differentiation
3 0 2 0.22 0 0
CUI: C4023190
Disease: Thyroid hemiagenesis
Thyroid hemiagenesis
9 0 3 0.21 0 0
CUI: C0014856
Disease: Esophageal Fistula
Esophageal Fistula
5 0 2 0.18 0 0
CUI: C1321809
Disease: HYPOTHYROIDISM, GOITROUS
HYPOTHYROIDISM, GOITROUS
5 0 2 0.18 0 0
CUI: C3715197
Disease: Primary congenital hypothyroidism
Primary congenital hypothyroidism
6 0 2 0.17 0 0
CUI: C0151516
Disease: Thyroid Hypoplasia
Thyroid Hypoplasia
14 0 3 0.16 0 0
CUI: C0342162
Disease: Compensated hypothyroidism
Compensated hypothyroidism
7 0 2 0.15 0 0
CUI: C2986550
Disease: Pituicytoma
Pituicytoma
7 0 2 0.15 0 0
Neuroendocrine cell hyperplasia of infancy
7 0 2 0.15 0 0
CUI: C1509148
Disease: Sclerosing hemangioma
Sclerosing hemangioma
8 0 2 0.14 0 0
CUI: C1563716
Disease: Thyroid Dysgenesis
Thyroid Dysgenesis
24 0 4 0.14 0 0
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3
8 0 2 0.14 0 0
CUI: C0271791
Disease: Severe hypothyroidism
Severe hypothyroidism
9 0 2 0.13 0 0
Stage IV Thyroid Gland Papillary Carcinoma AJCC v7
9 0 2 0.13 0 0
CUI: C0038478
Disease: Struma Ovarii
Struma Ovarii
10 0 2 0.12 0 0