Preferred Name

Paraparesis
Synonyms

Paraparesis (disorder)
ID

1845001
Full Id

http://purl.bioontology.org/ontology/SNOMEDCT/1845001
CONCEPTSTATUS

0
CTV3ID

Xa0fv
has_clinical_course

Courses
has_episodicity

Episodicities
has_finding_site

Structure of nervous system

Lower limb structure
has_severity

Severities
isa

Paralytic syndrome

Disorder of lower extremity
ISPRIMITIVE

1
Semantic_Type

Sign or Symptom
SNOMEDID

DA-26042
SYNONYM FN

Paraparesis (disorder)
TUI

T184
UMLS_CUI

C0221166
Create New Mapping

Mapping To Ontology Source Comment Relationship Added By Added On Notes
http://purl.bioontology.org/ontology/MDR/10033885 MedDRA NLM UMLS (CUI) CUI: C0221166 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/NDFRT/N0000004116 National Drug File NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://bioonto.de/mesh.owl#D020335 OWL Version of MeSH NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Paraparesis NCI Thesaurus NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/NDFRT/N0000004116 National Drug File NLM UMLS (CUI) CUI: C0221166 skos:closeMatch loom 04/02/13 View Notes
http://purl.org/obo/owl/MP#MP_0009434 Suggested Ontology for Pharmacogenomics NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/Xa0fv Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0221166 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MDR/10033885 MedDRA NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://www.ifomis.org/acgt/1.0#Paraparesis Cancer Research and Management ACGT Master Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.org/obo/owl/HP#HP_0002385 Bone Dysplasia Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://bioonto.de/mesh.owl#C10.597.636.500 OWL Version of MeSH NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.obolibrary.org/obo/HP_0002385 Human Phenotype Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.obolibrary.org/obo/MP_0009434 Mammalian phenotype NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:1918 Fanconi Anemia (FA) Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://bioonto.de/mesh.owl#C23.888.592.643.500 OWL Version of MeSH NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/ICD10CM/G82.2 ICD10CM NLM UMLS (CUI) CUI: C0221166 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU005587 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0221166 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/Xa0fv Read Codes, Clinical Terms Version 3 (CTV3) NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://www.owl-ontologies.com/OntologyXCT.owl#Paraparesis Cerebrotendinous xanthomatosis NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MSH/D020335 Medical Subject Headings (MeSH) NLM UMLS (CUI) CUI: C0221166 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU005587 Online Mendelian Inheritance in Man NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MSH/D020335 Medical Subject Headings (MeSH) NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes

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