loading...| Preferred Name |
autosomal dominant disease |
|
| Synonyms |
|
|
| Definitions |
An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_0050736 |
|
| created_by |
lschriml |
|
| creation_date |
2012-07-24T12:51:47Z |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:0050736 |
|
| imported from | ||
| label |
autosomal dominant disease |
|
| notation |
DOID:0050736 |
|
| prefLabel |
autosomal dominant disease |
|
| textual definition |
An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease. |
|
| subClassOf |
The BioAssay Ontology integrates with OntoloBridge, allowing community users to suggest additions to the public ontology. Complete the template below to submit a term request directly to the ontology maintainer.
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Example: Involves the use of a tissue derived from a living organism and is a heterogeneous assay type.
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