| Preferred Name |
Thyroid Dysgenesis |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C85190 |
| code |
C85190 |
| DEFINITION |
A congenital condition characterized by hypoplasia, absence, or ectopic position of the thyroid gland. It is manifested with congenital hypoparathyroidism. |
| label |
Thyroid Dysgenesis |
| Preferred_Name |
Thyroid Dysgenesis |
| prefixIRI |
C85190 |
| prefLabel |
Thyroid Dysgenesis |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C1563716 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/MESH/D050033 | Medical Subject Headings | LOOM |