Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Preferred Name

TORTICOLLIS

ID

http://purl.bioontology.org/ontology/OMIM/189600

cui

C0040485

MIMTYPEMEANING

Other, mainly phenotypes with suspected mendelian basis

notation

189600

OMIM Entry Type

0

OMIM MimType Value

none

prefLabel

TORTICOLLIS

tui

T184

Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bmicc.cn/ontology/ICD10CN/M43.6 International Classification of Diseases, 10th Edition, China CUI
http://purl.obolibrary.org/obo/HP_0000473 Human Phenotype Ontology LOOM
http://purl.bioontology.org/ontology/ICD10CM/M43.6 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/ICD10CM/M43.6 International Classification of Diseases, Version 10 - Clinical Modification LOOM
http://purl.bmicc.cn/ontology/ICD11CN/FA71 International Classification of Diseases, 11th Edition, China LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0040485 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0040485 MedlinePlus Health Topics LOOM
http://purl.obolibrary.org/obo/SYMP_0000617 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/ICD10/M43.6 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/ICD10/M43.6 International Classification of Diseases, Version 10 LOOM
http://purl.bioontology.org/ontology/MESH/D014103 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/D014103 Medical Subject Headings LOOM