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: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism
94 0 24 0.25 0 0
CUI: C2940786
Disease: Thyroid Hormone Resistance Syndrome
Thyroid Hormone Resistance Syndrome
25 0 7 0.16 0 0
CUI: C0749420
Disease: Thyroid Agenesis
Thyroid Agenesis
11 0 5 0.16 0 0
CUI: C1578691
Disease: Myxedema, Congenital
Myxedema, Congenital
4 0 4 0.15 0 0
CUI: C3715197
Disease: Primary congenital hypothyroidism
Primary congenital hypothyroidism
6 0 4 0.14 0 0
CUI: C0271791
Disease: Severe hypothyroidism
Severe hypothyroidism
9 0 4 0.13 0 0
CUI: C4023190
Disease: Thyroid hemiagenesis
Thyroid hemiagenesis
9 0 4 0.13 0 0
Generalized Thyroid Hormone Resistance
45 0 8 0.13 0 0
CUI: C0342191
Disease: Familial dyshormonogenetic goiter
Familial dyshormonogenetic goiter
11 0 4 0.12 0 0
CUI: C0027145
Disease: Myxedema
Myxedema
3 0 3 0.12 0 0
CUI: C0151516
Disease: Thyroid Hypoplasia
Thyroid Hypoplasia
14 0 4 0.11 0 0
CUI: C0342153
Disease: Congenital thyroid hypoplasia
Congenital thyroid hypoplasia
4 0 3 0.11 0 0
Growth Hormone Insensitivity Syndrome
4 0 3 0.11 0 0
CUI: C1321809
Disease: HYPOTHYROIDISM, GOITROUS
HYPOTHYROIDISM, GOITROUS
5 0 3 0.11 0 0
CUI: C1998045
Disease: Subclinical hyperthyroidism
Subclinical hyperthyroidism
5 0 3 0.11 0 0
CUI: C0271795
Disease: Transient hypothyroidism
Transient hypothyroidism
6 0 3 0.10 0 0
CUI: C1848805
Disease: Thyroid Dyshormonogenesis 1
Thyroid Dyshormonogenesis 1
6 0 3 0.10 0 0
CUI: C1855794
Disease: Bamforth syndrome
Bamforth syndrome
6 0 3 0.10 0 0
Transient hypothyroxinaemia of prematurity
6 0 3 0.10 0 0
CUI: C0271790
Disease: Subclinical hypothyroidism
Subclinical hypothyroidism
40 0 6 1.0E-01 0 0
CUI: C0342162
Disease: Compensated hypothyroidism
Compensated hypothyroidism
7 0 3 1.0E-01 0 0
CUI: C0349476
Disease: Congenital goiter
Congenital goiter
7 0 3 1.0E-01 0 0
CUI: C0016063
Disease: Osteitis Fibrosa Disseminata
Osteitis Fibrosa Disseminata
19 0 4 9.8E-02 0 0
CUI: C4316995
Disease: Primary Hypothyroidism
Primary Hypothyroidism
19 0 4 9.8E-02 0 0
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3
8 0 3 9.7E-02 0 0