hereditary inclusion-body myopathy
http://purl.obolibrary.org/obo/MONDO_0016112
Term info
database cross reference
- GARD:0001658 (MONDO:equivalentTo)
- Orphanet:206662 (MONDO:equivalentTo)
Subsets
gard_rare, disease_grouping, ordo_group_of_disorders
IAO 0000233
https://github.com/monarch-initiative/mondo/issues/5658
exactMatch
http://purl.obolibrary.org/obo/Orphanet_206662
has exact synonym
inclusion myopathy
has related synonym
cytoplasmic body myopathy
id
MONDO:0016112
seeAlso
https://rarediseases.info.nih.gov/diseases/1658/cytoplasmic-body-myopathy