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loading...| Preferred Name | Rare bone disease related to a common gene or pathway defect | |
| Synonyms |
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|
| ID |
http://www.orpha.net/ORDO/Orphanet_364803 |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=364803 |
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| hasDbXref |
UMLS:C5680975 |
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| label |
Rare bone disease related to a common gene or pathway defect |
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| notation |
ORPHA:364803 Category |
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| prefixIRI |
ORDO:Orphanet_364803 |
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| prefLabel |
Rare bone disease related to a common gene or pathway defect |
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| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://www.orpha.net/ORDO/Orphanet_364803 | CCONT | SAME_URI | |
| http://www.orpha.net/ORDO/Orphanet_364803 | EFO | SAME_URI | |
| http://www.orpha.net/ORDO/Orphanet_364803 | CCONT | LOOM | |
| http://www.orpha.net/ORDO/Orphanet_364803 | EFO | LOOM |