autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect
http://purl.obolibrary.org/obo/MONDO_0033850
Term info
database cross reference
- Orphanet:521411 (MONDO:equivalentTo)
Subsets
ordo_disease
exactMatch
http://purl.obolibrary.org/obo/Orphanet_521411
id
MONDO:0033850