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progressive supranuclear palsy

Go to external page http://purl.obolibrary.org/obo/MONDO_0019037

A rare late-onset neurodegenerative disease characterized by supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia. [ Orphanet:683 https://orcid.org/0000-0001-5208-3432 ]

Synonyms: Steele-Richardson-Olszewski disease Steele-Richardson-Olszewski syndrome progressive supranuclear ophthalmoplegia PSP syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • NORD:1619 (MONDO:NORD)
  • MEDGEN:21026 (MONDO:equivalentTo)
  • NANDO:1200009 (https://orcid.org/0000-0003-0011-764X)
  • icd11.foundation:1493396558 (Orphanet:683)
  • NCIT:C85028 (MONDO:equivalentTo)
  • MedDRA:10036813 (Orphanet:683/e)
  • Orphanet:683 (MONDO:equivalentTo)
  • SCTID:192976002 (MONDO:equivalentTo)
  • ICD9:333.0 (MONDO:relatedTo)
  • SCTID:28978003 (MONDO:relatedTo)
  • GARD:7471 (MONDO:GARD)
  • MESH:D013494 (Orphanet:683/e)
  • UMLS:C0038868 (MONDO:equivalentTo)
  • DOID:678 (MONDO:equivalentTo)
  • OMIMPS:601104 (MONDO:equivalentTo)
Subsets

ordo_disorder, gard_rare, matrix_llm__is_cancer_other, mondo_top_grouping_disorder_of_visual_system, mondo_top_grouping_member, matrix_llm__txgnn_other, nord_rare, matrix_included, matrix_txgnn_grouping_member, rare, orphanet_rare, mondo_top_grouping_syndromic_disease, harrisons_view_nervous_system_disorder, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, harrisons_view_disorder_of_visual_system, matrix_txgnn_grouping_neurodegenerative_disease, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease

closeMatch

http://identifiers.org/meddra/10036813

exactMatch

http://identifiers.org/snomedct/192976002

http://identifiers.org/medgen/21026

http://identifiers.org/mesh/D013494

https://omim.org/phenotypicSeries/PS601104

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

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

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

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

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1493396558

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0024237

http://purl.obolibrary.org/obo/MONDO_0015547

has related synonym

supranuclear palsy, progressive

familial progressive supranuclear palsy (type)

id

MONDO:0019037

relatedMatch

http://identifiers.org/snomedct/28978003

should conform to

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

term tracker item

https://github.com/monarch-initiative/mondo/issues/3100