Item:Q17589: Difference between revisions
Created a new Item: copper metabolism disease, Human disease |
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_309839 |
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| aliases / en / 0 | aliases / en / 0 | ||
inborn error of cellular copper ion homeostasis | |||
| aliases / en / 1 | aliases / en / 1 | ||
obsolete copper metabolism disease | |||
| Property / instance of | |||
| Property / instance of: class of disease / rank | |||
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| Property / subclass of | |||
| Property / subclass of: mineral metabolism disease / rank | |||
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| Property / subclass of | |||
| Property / subclass of: copper in biology / rank | |||
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| Property / exact match | |||
| Property / exact match: http://www.orpha.net/ORDO/Orphanet_309839 / rank | |||
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