An instance of peripheral neuropathy that is caused by an inherited genomic modification in an individual.

Synonyms: hereditary peripheral neuropathy genetic peripheral neuropathy

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:98497 (MONDO:equivalentTo)
  • GARD:10711 (Orphanet:98497)
Subsets

gard_rare, disease_grouping, rare, orphanet_rare, clingen, ordo_group_of_disorders

IAO 0000233

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

exactMatch

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

id

MONDO:0020127

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0020127

Term relations