An inherited disorder characterized by progressive degeneration and atrophy of the nervous system. [ NCIT:C97073 ]

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:183500 (MONDO:equivalentTo)
  • UMLS:CN200549 (MONDO:equivalentTo)
  • MESH:D020271 (MONDO:equivalentTo)
  • UMLS:C3273225 (NCIT:C97073)
  • NCIT:C97073 (MONDO:equivalentTo)
Subsets

ordo_group_of_disorders

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml

definition

An inherited disorder characterized by progressive degeneration and atrophy of the nervous system.

exactMatch

http://linkedlifedata.com/resource/umls/id/CN200549

http://identifiers.org/mesh/D020271

http://purl.obolibrary.org/obo/NCIT_C97073

http://linkedlifedata.com/resource/umls/id/C3273225

http://www.orpha.net/ORDO/Orphanet_183500

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0002320

has exact synonym

hereditary neurodegenerative disease

genetic neurodegenerative disease

hereditary neurodegenerative disorder

id

MONDO:0024237