Preferred Name

纯红细胞再生障碍 / Pure red cell aplasia

Definitions

A condition caused by determinates arising during the antenatal period, after birth or genetically inherited factors, leading to a change in the formation of erythrocytes. This condition is characterised by maturation arrest occurs in the formation of erythrocytes. This condition may present with severe anaemia. Confirmation is by identification of abnormally formed erythrocytes in a blood sample.

ID

http://purl.bmicc.cn/ontology/ICD11CN/L2-3A6

definition

A condition caused by determinates arising during the antenatal period, after birth or genetically inherited factors, leading to a change in the formation of erythrocytes. This condition is characterised by maturation arrest occurs in the formation of erythrocytes. This condition may present with severe anaemia. Confirmation is by identification of abnormally formed erythrocytes in a blood sample.

hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/1980066564

label

纯红细胞再生障碍 / Pure red cell aplasia

mappingRelation

http://purl.bmicc.cn/ontology/ICD10CN/D64.9

notation

L2-3A6

prefixIRI

ICD11CN:L2-3A6

prefLabel

纯红细胞再生障碍 / Pure red cell aplasia

subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/L1-3A0

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http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34974 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.obolibrary.org/obo/MONDO_0001705 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0001705 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/DOID_1340 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_1340 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.obolibrary.org/obo/HP_0012410 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/HP_0012410 Human Phenotype Ontology / 人类表型本体 LOOM