细胞系本体（中文翻译） / Cell Line Ontology (Chinese Translation) - 遗传性疾病

Preferred Name	遗传性疾病
ID	http://purl.obolibrary.org/obo/DOID_630
prefixIRI	DOID:630
prefLabel	遗传性疾病
seeAlso	UMLS_CUI:C0019247 NCI2009_04D:C3101 URI: http://www.ebi.ac.uk/cellline#hereditary_disease SNOMEDCT_2010_1_31:264530000 MSH2010_2010_02_22:D030342 SNOMEDCT_2010_1_31:32895009
引自	http://purl.obolibrary.org/obo/clo.owl
替代术语	“分子疾病” EXACT [NCI2004_11_17：C3101] “遗传性疾病（紊乱）” EXACT [SNOMEDCT_2005_07_31：32895009] “遗传性疾病” EXACT [SNOMEDCT_2005_07_31：264530000] “遗传性紊乱” EXACT [CSP2005：1254-7727]
标签	遗传性疾病
subClassOf	http://www.ebi.ac.uk/efo/EFO_0000408

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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/DOID_630	Cardiovascular Disease Ontology / 心血管疾病本体	SAME_URI
http://purl.obolibrary.org/obo/DOID_630	BioAssay Ontology / 生物活性分析本体	SAME_URI
http://purl.obolibrary.org/obo/DOID_630	Ontology of Drug Adverse Events / 药物不良反应本体	SAME_URI
http://purl.obolibrary.org/obo/DOID_630	Cell Line Ontology Subset for Chinese National Infrastructure of Cell Line Resource (NICR) / 国家实验细胞资源共享服务平台(NICR)细胞系本体子集	SAME_URI
http://purl.obolibrary.org/obo/DOID_630	Coronavirus Infectious Disease Ontology / 冠状病毒感染性疾病本体	SAME_URI
http://purl.obolibrary.org/obo/DOID_630	Human Disease Ontology / 人类疾病本体	SAME_URI