monogenic disease (Q12895): Difference between revisions
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Created claim: subclass of (P1): genetic disease (Q12896) |
Created claim: exact match (P409): http://identifiers.org/doid/DOID:0050177 |
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| (2 intermediate revisions by the same user not shown) | |||
| Property / has cause | |||
| Property / has cause: single gene mutation / rank | |||
Normal rank | |||
| Property / exact match | |||
| Property / exact match: http://purl.obolibrary.org/obo/DOID_0050177 / rank | |||
Normal rank | |||
| Property / exact match | |||
| Property / exact match: http://identifiers.org/doid/DOID:0050177 / rank | |||
Normal rank | |||
Latest revision as of 13:35, 30 June 2023
Human disease
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | monogenic disease |
Human disease |