loading...| Preferred Name |
simple genetic disease |
| Definitions |
“遗传性疾病是一种或多种异常等位基因的结果，可能是显性的（异常等位基因的单一拷贝足以引起疾病），半显性或隐性的（需要基因的两个拷贝有异常的等位基因）“。 [DO：WK，LS] "A hereditary 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)." [DO:wk,ls] |
| ID |
http://purl.obolibrary.org/obo/DOID_0050177 |
| comment |
“遗传性疾病是一种或多种异常等位基因的结果，可能是显性的（异常等位基因的单一拷贝足以引起疾病），半显性或隐性的（需要基因的两个拷贝有异常的等位基因）“。 [DO：WK，LS] "A hereditary 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)." [DO:wk,ls] |
| label |
simple genetic disease 简单遗传疾病 |
| prefixIRI |
DOID:0050177 |
| prefLabel |
simple genetic disease |
| seeAlso | |
| 引自 | |
| subClassOf |