Term info
database cross reference
- Orphanet:183500 (MONDO:equivalentTo)
- NCIT:C97073 (MONDO:equivalentTo)
- MESH:D020271 (MONDO:equivalentTo)
- UMLS:C3273225 (NCIT:C97073)
- UMLS:CN200549 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
An inherited disorder characterized by progressive degeneration and atrophy of the nervous system.
exactMatch
http://linkedlifedata.com/resource/umls/id/CN200549, http://purl.obolibrary.org/obo/NCIT_C97073, http://identifiers.org/mesh/D020271, http://purl.obolibrary.org/obo/Orphanet_183500, http://linkedlifedata.com/resource/umls/id/C3273225
excluded subClassOf
http://purl.obolibrary.org/obo/MONDO_0002320
has exact synonym
hereditary neurodegenerative disease, genetic neurodegenerative disease, hereditary neurodegenerative disorder
id
MONDO:0024237