Link to this page
Disease core ontology applied to Rare Diseases
Last uploaded:
February 7, 2014
Jump to:
| Preferred Name | Rare genetic thyroid disease | |
| Synonyms |
|
|
| ID |
http://www.limics.org/hrdo/rdfns#pat_id_18294 |
|
| id_Orpha |
183631
|
|
| patType |
group of phenomes
|
|
| prefixIRI |
hrdo:pat_id_18294
|
|
| prefLabel |
Rare genetic thyroid disease
|
|
| subClassOf |
Add comment
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |
Create mapping
| Mapping To | Ontology | Source |
|---|---|---|
| http://www.orpha.net/ORDO/Orphanet_183631 | CCONT | LOOM |
| http://www.orpha.net/ORDO/Orphanet_183631 | EFO | LOOM |
| http://www.orpha.net/ORDO/Orphanet_183631 | ORDO | LOOM |