Preferred Name

Paralysis

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3310

ALT_DEFINITION

Partial or complete loss of function of one or more muscles. It is usually caused by damage to the nervous system.

Loss of ability to move all or part of the body.

code

C3310

Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C62596

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

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C54450

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C99147

Contributing_Source

NICHD

FDA

DEFINITION

Partial or complete loss of function of one or more muscles. It is usually caused by damage to the nervous system.

FDA_Table

Patient Code (Appendix B)

FULL_SYN

Paralytic Syndrome

paralysis

Paralysis

label

Paralysis

Legacy Concept Name

Paralysis

Preferred_Name

Paralysis

prefixIRI

Thesaurus:C3310

prefLabel

Paralysis

Semantic_Type

Finding

UMLS_CUI

C0522224

xRef

IMDRF:E012202

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C5039

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http://purl.bioontology.org/ontology/LNC/MTHU051472 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.obolibrary.org/obo/SYMP_0000030 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0522224 MedlinePlus Health Topics / MedlinePlus网站健康主题 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU014551 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/HP_0003470 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/HP_0003470 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.obolibrary.org/obo/HP_0003470 GenEpiO / 基因组流行病学本体 LOOM
http://purl.bioontology.org/ontology/LNC/LP202888-6 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.bioontology.org/ontology/LNC/LA17344-5 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.bioontology.org/ontology/MESH/D010243 Medical Subject Headings / 医学主题词表 LOOM
http://purl.obolibrary.org/obo/NBO_0000032 中国人类表型本体 / Human Phenotype Ontology China LOOM
http://purl.bmicc.cn/ontology/HPCH/HP_0003470 中国人类表型本体 / Human Phenotype Ontology China LOOM