Jump to:
loading...| Preferred Name |
Rare genetic thyroid disease |
|
| Synonyms |
|
|
| ID |
http://www.orpha.net/ORDO/Orphanet_183631 |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=183631 |
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| hasDbXref |
UMLS:C5680539 |
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| label |
Rare genetic thyroid disease |
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| notation |
ORPHA:183631 Category |
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| prefixIRI |
ORDO:Orphanet_183631 |
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| prefLabel |
Rare genetic thyroid disease |
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| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://www.orpha.net/ORDO/Orphanet_183631 | EFO | SAME_URI | |
| http://www.limics.org/hrdo/rdfns#pat_id_18294 | HRDO | LOOM | |
| http://www.orpha.net/ORDO/Orphanet_183631 | EFO | LOOM |