disease arises from feature disease has basis in feature disease has feature Frontotemporal dementia syndromic disease movement disorder neurodegenerative disease hereditary dementia progressive supranuclear palsy https://github.com/monarch-initiative/mondo/issues/3100 https://github.com/monarch-initiative/mondo/issues/9097 https://github.com/monarch-initiative/mondo/issues/9285 https://www.malacards.org/card/progressive_supranuclear_palsy UMLS:C0038868 A rare late-onset neurodegenerative disease characterized by supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia. NORD:1619 supranuclear palsy, progressive progressive supranuclear ophthalmoplegia ICD9:333.0 NANDO:1200009 Orphanet:683 SCTID:28978003 SCTID:192976002 MONDO:0019037 MESH:D013494 Steele-Richardson-Olszewski disease ICD10CM:G23.1 MEDGEN:21026 Steele-Richardson-Olszewski syndrome NCIT:C85028 GARD:0007471 OMIMPS:601104 familial progressive supranuclear palsy (type) icd11.foundation:1493396558 PSP syndrome MedDRA:10036813 DOID:678 supranuclear oculomotor palsy inherited neurodegenerative disorder