progressive supranuclear palsy
A rare late-onset neurodegenerative disease characterized by supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia. [ https://orcid.org/0000-0001-5208-3432 Orphanet:683 ]
Term info
- GARD:0007471 (MONDO:equivalentTo)
- ICD9:333.0 (MONDO:relatedTo)
- UMLS:CN205522 (MONDO:equivalentTo)
- NCIT:C85028 (MONDO:equivalentTo)
- UMLS:C0038868 (Orphanet:683/e)
- Orphanet:683 (MONDO:equivalentTo)
- MESH:D013494 (Orphanet:683/e)
- MedDRA:10036813 (Orphanet:683/e)
- SCTID:28978003 (MONDO:relatedTo)
- DOID:678 (MONDO:equivalentTo)
- SCTID:192976002 (MONDO:equivalentTo)
ordo_disease
http://identifiers.org/meddra/10036813
A rare late-onset neurodegenerative disease characterized by supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia.
http://identifiers.org/snomedct/192976002, http://linkedlifedata.com/resource/umls/id/CN205522, http://identifiers.org/mesh/D013494, http://purl.obolibrary.org/obo/Orphanet_683, http://purl.obolibrary.org/obo/NCIT_C85028, http://linkedlifedata.com/resource/umls/id/C0038868, http://purl.obolibrary.org/obo/DOID_678
http://purl.obolibrary.org/obo/MONDO_0024237, http://purl.obolibrary.org/obo/MONDO_0015547
progressive supranuclear ophthalmoplegia, PSP syndrome
Steele-Richardson-Olszewski syndrome
supranuclear palsy, progressive, familial progressive supranuclear palsy (type)
MONDO:0019037
http://identifiers.org/snomedct/28978003