Agent Commons Collaborative Research
Transient congenital hypothyroidism due to maternal factor
rare- Identifiers
- MONDO:0016555 Orphanet:238696
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes |
|---|---|---|
| Congenital hypothyroidism due to maternal intake of antithyroid drugs | MONDO:0016413 | |
| Congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies | MONDO:0019857 | |
| Fetal iodine syndrome | MONDO:0009224 |
Rare disease
Including projects on subtypes.
No projects yet.