Jump to:
loading...| Preferred Name |
Congenital Hypothyroidism [Disease/Finding] |
|
| Synonyms |
Congenital Hypothyroidism Cretinism |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000171688 |
|
| altLabel |
Congenital Hypothyroidism Cretinism |
|
| cui |
C0010308 |
|
| MESH DEFINITION |
A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA. |
|
| MESH DUI |
D003409 |
|
| MeSH name |
Congenital Hypothyroidism |
|
| MESH UI |
M0005308 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000171688 |
|
| NUI |
N0000171688 |
|
| prefLabel |
Congenital Hypothyroidism [Disease/Finding] |
|
| SNOMED CID |
190268003 |
|
| tui |
T047 |
|
| subClassOf |
Create mapping