autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
Go to external page http://purl.obolibrary.org/obo/MONDO_0018567
Synonyms: CMT2 due to TFG mutation
This is just here as a test because I lose it
Term information
database
cross reference
- GARD:21815 (MONDO:GARD)
- UMLS:C5569028 (MONDO:equivalentTo)
- MEDGEN:1800451 (MONDO:equivalentTo)
- Orphanet:435819 (MONDO:equivalentTo)
Subsets
gard_rare, ordo_disorder, rare, nord_rare, orphanet_rare
exactMatch
http://linkedlifedata.com/resource/umls/id/C5569028
http://identifiers.org/medgen/1800451
http://www.orpha.net/ORDO/Orphanet_435819