autosomal dominant disease (Q21252): Difference between revisions
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Created a new Item: autosomal dominant disease, genetic disease characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease |
Created claim: exact match (P409): http://identifiers.org/doid/DOID:0050736 |
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| Property / instance of | |||
| Property / instance of: class of disease / rank | |||
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| Property / subclass of | |||
| Property / subclass of: autosomal genetic disease / rank | |||
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| Property / has cause | |||
| Property / has cause: autosomal dominant / rank | |||
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| Property / exact match | |||
| Property / exact match: http://purl.obolibrary.org/obo/DOID_0050736 / rank | |||
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| Property / exact match | |||
| Property / exact match: http://identifiers.org/doid/DOID:0050736 / rank | |||
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Latest revision as of 10:33, 28 February 2024
genetic disease characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease
- autosomal dominant inherited disorder
- autosomal dominant hereditary disorder
- disease, autosomal dominant
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant disease |
genetic disease characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease |
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