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Preferred Name

Pure Red Cell Aplasia
ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34974
ALT_DEFINITION

A condition characterized by aplasia of the erythroid series only. The leukocytes and platelets are not affected.
code

C34974
Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C132009
Contributing_Source

NICHD
DEFINITION

A disease characterized by normocytic, normochromic anemia, low hematocrit, reticulocytopenia, and selective erythroid hypoplasia.
FULL_SYN

PRCA

Pure Red Cell Aplasia
label

Pure Red Cell Aplasia
Legacy Concept Name

Pure_Red_Cell_Aplasia
Preferred_Name

Pure Red Cell Aplasia
prefixIRI

Thesaurus:C34974
prefLabel

Pure Red Cell Aplasia
Semantic_Type

Disease or Syndrome
UMLS_CUI

C0034902
subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26324
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Delete Mapping To Ontology Source
http://purl.bmicc.cn/ontology/ICD11CN/L2-3A6 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China 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 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