JSON

hereditary peripheral neuropathy

Go to external page http://purl.obolibrary.org/obo/MONDO_0020127

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

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, disease_grouping, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_included, clingen, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease, ordo_group_of_disorders, harrisons_view_nervous_system_disorder

contributor

https://orcid.org/0000-0002-4142-7153

https://orcid.org/0000-0003-2955-4640

curated content resource

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

exactMatch

http://identifiers.org/medgen/1825937

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

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

id

MONDO:0020127

term tracker item

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