ORPHA:238688
Neonatal iodine exposure
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Infancy, Neonatal
- Status
- active
Neonatal iodine exposure is a rare endocrine disease characterized by the appearance of transient hypothyroidism, usually in preterm newborns, following long or short-term topical iodine exposure. Parenteral exposure from iodinated contrast agents may similarly alter thyroid function in term neonates.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Neonatal iodine exposure | |
| fr | Exposition néonatale à l'iode | |
| de | Neonatale Jodexposition | |
| es | Exposición neonatal al yodo | |
| it | Esposizione neonatale allo iodio | |
| nl | Neonatale blootstelling aan jodium | |
| pt | Exposição neonatal a iodo | |
| pl | Nadmierna ekspozycja na jod w okresie noworodkowym | |
| cs | Novorozenecká expozice jódu | |
| uk | Вплив йоду на новонароджених | |
| zh | 新生儿碘暴露 | |
| tr | Yenidoğan iyot maruziyeti |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | P72.2 | NTBT | attributed | validated |
| ICD-11 | 5A00.03 | NTBT | index | validated |
| MONDO | 0016554 | E | validated | |
| UMLS | C4751432 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:238699Transient congenital hypothyroidism due to neonatal factor
rare endocrine diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/238688
- This record as JSON: /data/d/238688.json