Progressive supranuclear palsy (PSP) is a rare late-onset neurodegenerative disease characterized by supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia. [ Orphanet:683 ]

This is just here as a test because I lose it

Term information

database cross reference
  • SCTID:28978003 (MONDO:equivalentTo)
  • MESH:D013494 (Orphanet:683)
  • UMLS:CN205522 (MONDO:equivalentTo)
  • ICD9:333.0 (i2s)
  • NCIT:C85028 (MONDO:equivalentTo)
  • GARD:0007471 (Orphanet-shared)
  • ICD10:G23.1 (Orphanet:683)
  • UMLS:C0038868 (Orphanet:683)
  • DOID:678 (MONDO:equivalentTo)
  • MedDRA:10036813 (Orphanet:683)
  • Orphanet:683 (MONDO:equivalentTo)
Subsets

ordo_disease

closeMatch

http://identifiers.org/snomedct/192976002

http://identifiers.org/snomedct/192975003

definition

Progressive supranuclear palsy (PSP) is a rare late-onset neurodegenerative disease characterized by supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia.

exactMatch

http://linkedlifedata.com/resource/umls/id/CN205522

http://identifiers.org/mesh/D013494

http://purl.obolibrary.org/obo/NCIT_C85028

http://identifiers.org/meddra/10036813

http://linkedlifedata.com/resource/umls/id/C0038868

http://identifiers.org/snomedct/28978003

http://purl.obolibrary.org/obo/DOID_678

http://www.orpha.net/ORDO/Orphanet_683

has exact synonym

Steele-Richardson-Olszewski syndrome

progressive supranuclear ophthalmoplegia

PSP syndrome

has related synonym

supranuclear palsy, progressive

familial progressive supranuclear palsy (type)

id

MONDO:0019037