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Orphanet Rare Disease Ontology
Last uploaded:
July 3, 2024
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| Preferred Name | Rare hypothyroidism | |
| Synonyms |
|
|
| ID |
http://www.orpha.net/ORDO/Orphanet_181396 |
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=181396 |
|
| hasDbXref |
UMLS:C5680612
|
|
| label |
Rare hypothyroidism
|
|
| notation |
ORPHA:181396 Category
|
|
| prefixIRI |
ORDO:Orphanet_181396
|
|
| prefLabel |
Rare hypothyroidism
|
|
| subClassOf |
http://www.orpha.net/ORDO/Orphanet_557492 |
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| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |
Create mapping
| Mapping To | Ontology | Source |
|---|---|---|
| http://www.orpha.net/ORDO/Orphanet_181396 | CCONT | SAME_URI |
| http://www.orpha.net/ORDO/Orphanet_181396 | EFO | SAME_URI |
| http://www.orpha.net/ORDO/Orphanet_181396 | CCONT | LOOM |
| http://www.orpha.net/ORDO/Orphanet_181396 | EFO | LOOM |
| http://www.limics.org/hrdo/rdfns#pat_id_18177 | HRDO | LOOM |