| Label | Id | |
|---|---|---|
| TDH2A | 10133 | |
| hypothyroidism, congenital, due to dyshormonogenesis, 2A | 10133 | |
| thyroid dyshormonogenesis 2A | 10133 | |
| thyroid dyshormonogenesis 2A; TDH2A | http://purl.obolibrary.org/obo/MONDO_0010133 | |
| iodide peroxidase deficiency | 10133 | |
| thyroid peroxidase deficiency | 10133 | |
| familial thyroid dyshormonogenesis caused by mutation in TPO | 10133 | |
| thyroid hormonogenesis, genetic defect in, 2A | 10133 | |
| TPO familial thyroid dyshormonogenesis | 10133 | |
| thyroid dyshormonogenesis type 2A | 10133 |