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

URI: http://www.ebi.ac.uk/cellline#simple_genetic_disease

引自

http://purl.obolibrary.org/obo/clo.owl

subClassOf

http://purl.obolibrary.org/obo/DOID_630

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_0050177 International Classification of Diseases Ontology SAME_URI
http://purl.obolibrary.org/obo/DOID_0050177 Cell Line Ontology (Chinese Translation) SAME_URI
http://purl.obolibrary.org/obo/DOID_0050177 Human Disease Ontology 123 SAME_URI