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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) 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:Distal Hereditary Motor Neuronopathy Type 5C
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Accession:DOID:9006235 term browser browse the term
Status:
This term is obsolete.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: DHMN VC;   DHMN5C;   DSMA5C;   DSMAVC;   HMN5C;   HMND13;   distal hereditary motor neuronopathy type VC;   distal hereditary motor neuronopathy, Harding type VC;   distal hereditary motor neuronopathy, autosomal dominant 13;   distal hereditary motor neuropathy type VC;   distal hereditary motor neuropathy, Harding type VC;   distal spinal muscular atrophy type 5C;   distal spinal muscular atrophy type VC;   distal spinal muscular atrophy, Harding type VC
 replaced_by: DOID:0081401


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