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Browse result for Thyroid dyshormonogenesis
※ introduction Approximately 10% of patients with congenital hypothyroidism harbor inborn errors of metabolism in one of the steps for thyroid hormone synthesis in thyrocytes (Vono-Toniolo et al., 2005). Dyshormonogenesis can be caused by recessive defects at any of the steps required for normal thyroid hormone synthesis. In untreated patients thyroid dyshormonogenesis is typically associated with goitrous enlargement of the thyroid secondary to long-term thyrotropin (TSH; see 188540) stimulation.
Reference
OMIM: Thyroid dyshormonogenesis
Reference
OMIM: Thyroid dyshormonogenesis
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD03813 | P07202 | 7173 | TPO | Thyroid peroxidase | Homo sapiens |
| PTMD08316 | Q6PHW0 | 38943 | IYD | Iodotyrosine deiodinase 1 | Homo sapiens |
