Jump to:
loading...| Preferred Name |
Rare genetic hepatic disease |
|
| Synonyms |
|
|
| ID |
http://www.orpha.net/ORDO/Orphanet_156601 |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=156601 |
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| hasDbXref |
UMLS:C5680645 |
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| label |
Rare genetic hepatic disease |
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| notation |
ORPHA:156601 Category |
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| prefixIRI |
ORDO:Orphanet_156601 |
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| prefLabel |
Rare genetic hepatic disease |
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| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://www.orpha.net/ORDO/Orphanet_156601 | EFO | SAME_URI | |
| http://www.orpha.net/ORDO/Orphanet_156601 | EFO | LOOM | |
| http://www.limics.org/hrdo/rdfns#pat_id_17122 | HRDO | LOOM |