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
  • UMLS:C5681733 (MONDO:equivalentTo)
  • Orphanet:98497 (MONDO:equivalentTo)
  • GARD:10711 (MONDO:GARD)
  • MEDGEN:1825937 (MONDO:equivalentTo)
Subsets

gard_rare, otar, disease_grouping, rare, clingen, ordo_group_of_disorders

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/5114

exactMatch

http://identifiers.org/medgen/1825937

http://linkedlifedata.com/resource/umls/id/C5681733

http://www.orpha.net/ORDO/Orphanet_98497

id

MONDO:0020127