Term info
database cross reference
- UMLS:CN204832 (MONDO:equivalentTo)
- Orphanet:370034 (MONDO:equivalentTo)
Subsets
ordo_clinical_subtype
definition
An instance of syringomyelia that is caused by an inherited modification of the individual's genome.
exactMatch
http://purl.obolibrary.org/obo/Orphanet_370034, http://linkedlifedata.com/resource/umls/id/CN204832
has exact synonym
hereditary syringomyelia
id
MONDO:0018257