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 |

