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Hypertension Ontology
Last uploaded:
September 4, 2019
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| Id | http://purl.obolibrary.org/obo/DOID_0050177
http://purl.obolibrary.org/obo/DOID_0050177
|
|---|---|
| Preferred Name | monogenic disease |
| Definitions |
A genetic disease that is the result of one or more abnormal alleles and may be dominant (a single copy of the abnormal allele is sufficient to give rise to the disease), semi-dominant, or recessive (requiring both copies of the gene to have an abnormal allele).
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| label |
monogenic disease
|
|---|---|
| prefLabel |
monogenic disease
|
| notation |
DOID:0050177
|
| id |
DOID:0050177
|
| has_obo_namespace |
disease_ontology
|
| textual definition |
A genetic disease that is the result of one or more abnormal alleles and may be dominant (a single copy of the abnormal allele is sufficient to give rise to the disease), semi-dominant, or recessive (requiring both copies of the gene to have an abnormal allele).
|
| subClassOf | |
| imported from | |
| type |
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