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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Inclusion Body Myopathy 3, Autosomal Dominant
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Accession:DOID:9008434 term browser browse the term
This term is obsolete. We suggest searching for the text of the ontology term or for a keyword rather than searching for the ontology ID. For more information, please contact us.
Synonyms:exact_synonym: IBM3;   INCLUSION BODY MYOPATHY, DOMINANT;   Inclusion Body Myopathy, Autosomal Dominant;   Inclusion body myopathy 3;   MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA;   MYPOP;   Myopathy with Congenital Joint Contractures, Ophthalmoplegia, and Rimmed Vacuoles
 alt_id: OMIM:605637;   RDO:0004294
 replaced_by: DOID:0080719
For additional species annotation, visit the Alliance of Genome Resources.

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.