An instance of peripheral neuropathy that is caused by an inherited genomic modification in an individual.
Synonyms: genetic peripheral neuropathy
This is just here as a test because I lose it
Term information
database
cross reference
- GARD:10711 (MONDO:GARD)
- UMLS:C5681733 (MONDO:equivalentTo)
- Orphanet:98497 (MONDO:equivalentTo)
- MEDGEN:1825937 (MONDO:equivalentTo)
Subsets
gard_rare, otar, disease_grouping, rare, clingen, ordo_group_of_disorders
exactMatch
http://identifiers.org/medgen/1825937
http://linkedlifedata.com/resource/umls/id/C5681733
http://www.orpha.net/ORDO/Orphanet_98497