Congenital hypothyroidism
Congenital hypothyroidism
Definition
A thyroid hormone deficiency present from birth.
Also known as congenital hypothyroidism, congenital iodine deficiency syndrome — per MONDO
Also identified as
- DOID 0050328 per MONDO
- ICD9 243 per MONDO
- ICD9 269.3 per MONDO
- ICD9 759.89 per MONDO
- MESH D003409 per MONDO
- NCIT C26734 per MONDO
- Orphanet 442 per MONDO
- SCTID 190268003 per MONDO
- SCTID 217710005 per MONDO
- UMLS C0010308 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Craniocervical region | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Craniocervical region | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Endocrine gland | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Neck | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Neck | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Thyroid gland | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Thyroid gland | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |