autosomal genetic disease (Q21253): Difference between revisions
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Created claim: instance of (P2): class of disease (Q5294) |
Created claim: exact match (P409): http://identifiers.org/doid/DOID:0050739 |
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| Property / subclass of | |||
| Property / subclass of: monogenic disease / rank | |||
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| Property / exact match | |||
| Property / exact match: http://purl.obolibrary.org/obo/DOID_0050739 / rank | |||
Normal rank | |||
| Property / exact match | |||
| Property / exact match: http://identifiers.org/doid/DOID:0050739 / rank | |||
Normal rank | |||
Latest revision as of 09:58, 28 February 2024
monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes
- autosomal inherited disorder
- autosomal hereditary disorder
- autosomal inherited disease
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal genetic disease |
monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes |
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