Source: ALL
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: C1863752
Disease: Enlarged Vestibular Aqueduct
Enlarged Vestibular Aqueduct 		4 0 3 0.38 0 0
CUI: C1862050
Disease: Cochlear malformation
Cochlear malformation 		5 0 3 0.33 0 0
CUI: C1998045
Disease: Subclinical hyperthyroidism
Subclinical hyperthyroidism 		5 0 3 0.33 0 0
CUI: C0749420
Disease: Thyroid Agenesis
Thyroid Agenesis 		11 0 4 0.29 0 0
CUI: C3163939
Disease: Malignant epithelial neoplasm of thyroid
Malignant epithelial neoplasm of thyroid 		2 0 2 0.29 0 0
CUI: C2676974
Disease: Hypoplasia of the cochlea
Hypoplasia of the cochlea 		7 0 3 0.27 0 0
CUI: C0700502
Disease: Acquired hypothyroidism
Acquired hypothyroidism 		13 0 4 0.25 0 0
CUI: C2607947
Disease: Unilateral deafness
Unilateral deafness 		3 0 2 0.25 0 0
CUI: C0342196
Disease: Thyroid Dyshormonogenesis 5
Thyroid Dyshormonogenesis 5 		4 0 2 0.22 0 0
CUI: C0038478
Disease: Struma Ovarii
Struma Ovarii 		10 0 3 0.21 0 0
CUI: C3538946
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT 		10 0 3 0.21 0 0
CUI: C0271826
Disease: Iodide transport defect
Iodide transport defect 		5 0 2 0.20 0 0
CUI: C0342191
Disease: Familial dyshormonogenetic goiter
Familial dyshormonogenetic goiter 		11 0 3 0.20 0 0
CUI: C3715197
Disease: Primary congenital hypothyroidism
Primary congenital hypothyroidism 		6 0 2 0.18 0 0
CUI: C4316995
Disease: Primary Hypothyroidism
Primary Hypothyroidism 		19 0 4 0.18 0 0
CUI: C0271829
Disease: Pendred's syndrome
Pendred's syndrome 		35 0 6 0.17 0 0
CUI: C0302859
Disease: Euthyroid Goiter
Euthyroid Goiter 		7 0 2 0.17 0 0
CUI: C0349476
Disease: Congenital goiter
Congenital goiter 		7 0 2 0.17 0 0
CUI: C2747905
Disease: Destructive thyroiditis
Destructive thyroiditis 		7 0 2 0.17 0 0
CUI: C0342199
Disease: Iodine deficiency syndrome
Iodine deficiency syndrome 		22 0 4 0.16 0 0
CUI: C0266283
Disease: Ectopic thyroid tissue (disorder)
Ectopic thyroid tissue (disorder) 		8 0 2 0.15 0 0
CUI: C2940785
Disease: HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3 		8 0 2 0.15 0 0
CUI: C1843865
Disease: Vestibular dysfunction
Vestibular dysfunction 		16 0 3 0.15 0 0
CUI: C0158983
Disease: Neonatal thyrotoxicosis
Neonatal thyrotoxicosis 		1 0 1 0.14 0 0
CUI: C0238185
Disease: Juvenile myxedema
Juvenile myxedema 		1 0 1 0.14 0 0