Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

SPONDYLOLISTHESIS
ID

http://purl.bioontology.org/ontology/OMIM/184200
cui

C0038016
MIMTYPEMEANING

Mendelian phenotype or locus, molecular basis unknown.
notation

184200
OMIM Entry Type

5
OMIM MimType Value

perc
prefLabel

SPONDYLOLISTHESIS
tui

T047
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http://purl.bioontology.org/ontology/ICD10CM/M43.1 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/ICD10CM/M43.1 International Classification of Diseases, Version 10 - Clinical Modification LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C35033 National Cancer Institute Thesaurus LOOM
http://purl.obolibrary.org/obo/HP_0003302 Human Phenotype Ontology LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0038016 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0038016 MedlinePlus Health Topics LOOM
http://purl.obolibrary.org/obo/DOID_6682 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/ICD10CM/M43.10 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/MESH/D013168 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/D013168 Medical Subject Headings LOOM
http://purl.bmicc.cn/ontology/ICD11CN/FA84 International Classification of Diseases, 11th Edition, China LOOM
http://purl.bioontology.org/ontology/ICD10/M43.1 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/ICD10/M43.1 International Classification of Diseases, Version 10 LOOM
http://purl.bmicc.cn/ontology/ICD10CN/M43.1 International Classification of Diseases, 10th Edition, China CUI