Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Ectopic thyroid tissue |
Is a |
False |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
Congenital hypothyroidism with ectopic thyroid |
Is a |
True |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
Congenital thyroid hypoplasia |
Is a |
True |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
Congenital atrophy of thyroid |
Is a |
False |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
Aberrant thyroid gland |
Is a |
True |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
Thyroglossal duct anomaly |
Is a |
False |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
Accessory thyroid gland |
Is a |
True |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
Congenital absence of thyroid gland |
Is a |
True |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
Congenital malposition of the thyroid gland |
Is a |
False |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
Anomalies of thyroid gland NEC |
Is a |
False |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
A very rare syndrome of congenital hypothyroidism characterized by thyroid dysgenesis (in most cases athyreosis), cleft palate and spiky hair, with or without choanal atresia, and bifid epiglottis. Facial dysmorphism and porencephaly have been reported in isolated cases. |
Is a |
True |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
Athyrotic hypothyroidism sequence |
Is a |
True |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
Multinodular goiter - cystic kidney - polydactyly syndrome is a very rare syndrome characterized by the association of multinodular goiter, cystic renal disease and digital anomalies. |
Is a |
True |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
Congenital iodine deficiency syndrome |
Is a |
True |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by choanal atresia, athelia or hypoplastic nipples, branchial arch abnormalities, external ear malformations, hearing loss, thyroid abnormalities, delayed or absent pubertal development, and short stature. Developmental delay/intellectual disability are variably reported. |
Is a |
True |
Congenital anomaly of the thyroid gland |
Inferred relationship |
Some |
|