Agent Commons Collaborative Research
Hypothyroidism, congenital, nongoitrous
rare- Identifiers
- MONDO:0000045
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Congenital nongoitrous hypothyroidism 3 | MONDO:0012360 | ||
| Congenital nongoitrous hypothyroidism 6 | MONDO:0013757 | THRA | |
| Hypothyroidism due to TSH receptor mutations | MONDO:0010142 | TSHR | |
| Hypothyroidism, congenital, nongoitrous, 2 | MONDO:0024264 | PAX8 | |
| Hypothyroidism, congenital, nongoitrous, 5 | MONDO:0009154 | NKX2-5 | |
| Hypothyroidism, congenital, nongoitrous, 7 | MONDO:0032819 | TRHR | |
| Hypothyroidism, congenital, nongoitrous, 8 | MONDO:0026731 | TBL1X | |
| Hypothyroidism, congenital, nongoitrous, 9 | MONDO:0026732 | IRS4 | |
| Isolated thyroid-stimulating hormone deficiency | MONDO:0010139 | TSHB |
Rare disease
Including projects on subtypes.
No projects yet.