Item:Q17610: Difference between revisions
Created claim: subclass of (P1): rare genetic hepatic disease (Q17576) |
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_101940 |
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Property / exact match | |||
Property / exact match: http://www.orpha.net/ORDO/Orphanet_101940 / rank | |||
Normal rank |