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Orphanet Rare Disease Ontology
Last uploaded:
July 3, 2024
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Preferred Name | Rare genetic cause of hypertension | |
Synonyms |
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ID |
http://www.orpha.net/ORDO/Orphanet_156629 |
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expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=156629 |
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hasDbXref |
UMLS:C5680639
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label |
Rare genetic cause of hypertension
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notation |
ORPHA:156629 Category
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prefixIRI |
ORDO:Orphanet_156629
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prefLabel |
Rare genetic cause of hypertension
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subClassOf |
http://www.orpha.net/ORDO/Orphanet_98056 |
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Delete | Subject | Author | Type | Created |
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Create mapping
Mapping To | Ontology | Source |
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http://www.orpha.net/ORDO/Orphanet_156629 | CCONT | SAME_URI |
http://www.orpha.net/ORDO/Orphanet_156629 | EFO | SAME_URI |