A hereditary spastic paraplegia that is part of a larger syndrome. [ MONDO:patterns/syndromic ]

Synonyms: complicated SPG Complex SPG syndrome associated with hereditary spastic paraplegia Complex familial spastic paraplegia complicated HSP Complex HSP complicated familial spastic paraplegia syndromic hereditary spastic paraplegia complicated hereditary spastic paraplegia

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:581446 (MONDO:equivalentTo)
  • SCTID:230261006 (MONDO:equivalentTo)
  • UMLS:C0393556 (MONDO:equivalentTo)
  • GARD:19823 (MONDO:GARD)
  • Orphanet:102013 (MONDO:equivalentTo)
  • NANDO:1200054 (https://orcid.org/0000-0003-0011-764X)
Subsets

matrix_llm__is_cancer_other, gard_rare, disease_grouping, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_included, clingen, matrix_txgnn_grouping_member, rare, harrisons_view_nervous_system_disorder, mondo_top_grouping_syndromic_disease, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, 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, ordo_group_of_disorders

curated content resource

https://search.clinicalgenome.org/kb/conditions/MONDO:0015150

exactMatch

http://identifiers.org/medgen/581446

http://linkedlifedata.com/resource/umls/id/C0393556

http://www.orpha.net/ORDO/Orphanet_102013

http://identifiers.org/snomedct/230261006

id

MONDO:0015150