List of diseases covered by
Hypothyroidism and Thyroid Hormone Resistance
NGS panel
Gene | Condition |
DUOX2 | Thyroid dyshormonogenesis 6 |
DUOXA2 | Thyroid dyshormonogenesis 5 |
GNAS | McCune-Albright syndrome; ACTH-independent macronodular adrenal hyperplasia; Pseudohypoparathyroidism Ia; Pseudohypoparathyroidism Ib; Pseudohypoparathyroidism Ic; Pseudopseudohypoparathyroidism; Osseous heteroplasia, progressive |
HESX1 | Pituitary hormone deficiency, combined, 5 |
IYD | Thyroid dyshormonogenesis 4 |
NKX2-1 | Choreoathetosis, hypothyroidism, and neonatal respiratory distress; Chorea, hereditary benign; Thyroid cancer, nonmedullary, 1 |
NKX2-5 | Hypothyroidism, congenital nongoitrous, 5; Atrial septal defect 7, with or without AV conduction defects; Conotruncal heart malformations, variable; Hypoplastic left heart syndrome 2; Tetralogy of Fallot; Ventricular septal defect 3 |
PAX8 | Hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia |
POU1F1 | Pituitary hormone deficiency, combined, 1 |
PROP1 | Pituitary hormone deficiency, combined, 2 |
SECISBP2 | Thyroid hormone metabolism, abnormal |
SLC5A5 | Thyroid dyshormonogenesis 1 |
SLC16A2 | Allan-Herndon-Dudley syndrome |
SLC26A4 | Pendred syndrome; Deafness, autosomal recessive 4, with enlarged vestibular aqueduct |
STX16 | Pseudohypoparathyroidism, type IB |
TG | Thyroid dyshormonogenesis 3; Autoimmune thyroid disease, susceptibility to, 3 |
THRA | Hypothyroidism, congenital, nongoitrous, 6 |
THRB | Thyroid hormone resistance; Thyroid hormone resistance, autosomal recessive; Thyroid hormone resistance, selective pituitary |
TPO | Thyroid dyshormonogenesis 2A |
TRHR | Thyrotropin-releasing hormone resistance, generalized |
TSHB | Hypothyroidism, congenital, nongoitrous 4 |
TSHR | Hyperthyroidism, familial gestational; Hyperthyroidism, nonautoimmune; Hypothyroidism, congenital, nongoitrous, 1 |