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 |