congenital hemolytic anemia (Q21845): Difference between revisions
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Created a new Item: congenital hemolytic anemia, Human disease |
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_182043 |
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| Property / instance of: class of disease / rank | |||
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| Property / instance of: symptom or sign / rank | |||
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| Property / subclass of: hemolytic anemia / rank | |||
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| Property / subclass of: congenital anemia / rank | |||
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| Property / health specialty: hematology / rank | |||
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| Property / exact match: http://purl.obolibrary.org/obo/DOID_589 / rank | |||
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| Property / exact match | |||
| Property / exact match: http://identifiers.org/doid/DOID:589 / rank | |||
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| Property / exact match: http://purl.obolibrary.org/obo/HP_0004804 / rank | |||
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| Property / exact match | |||
| Property / exact match: http://www.orpha.net/ORDO/Orphanet_182043 / rank | |||
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Latest revision as of 21:13, 6 April 2024
Human disease
- hereditary hemolytic anemia
- Anemia hemolytic congenital
- constitutional hemolytic anemia
- rare familial constitutional hemolytic anemia
- rare genetic constitutional hemolytic anemia
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital hemolytic anemia |
Human disease |
|