autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
http://purl.obolibrary.org/obo/MONDO_0018567
Term info
database cross reference
- Orphanet:435819 (MONDO:equivalentTo)
- UMLS:CN237576 (MONDO:equivalentTo)
Subsets
ordo_disease
exactMatch
http://linkedlifedata.com/resource/umls/id/CN237576, http://purl.obolibrary.org/obo/Orphanet_435819
has exact synonym
CMT2 due to TFG mutation
id
MONDO:0018567