JSON

[X] inherited neurodegenerative disorder

Go to external page http://purl.obolibrary.org/obo/MONDO_0024237

An inherited disorder characterized by progressive degeneration and atrophy of the nervous system. [ NCIT:C97073 ]

Synonyms: hereditary neurodegenerative disease genetic neurodegenerative disease hereditary neurodegenerative disorder

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:20280 (MONDO:GARD)
  • MEDGEN:1825988 (MONDO:equivalentTo)
  • MESH:D020271 (MONDO:equivalentTo)
  • NCIT:C97073 (MONDO:equivalentTo)
  • Orphanet:183500 (MONDO:equivalentTo)
  • UMLS:C5680568 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, disease_grouping, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, matrix_txgnn_grouping_neurodegenerative_disease, matrix_llm__tag_existing_treatment_other, clingen, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease, ordo_group_of_disorders, harrisons_view_nervous_system_disorder

contributor

https://orcid.org/0000-0003-2955-4640

curated content resource

https://search.clinicalgenome.org/kb/conditions/MONDO:0024237

exactMatch

http://identifiers.org/mesh/D020271

http://purl.obolibrary.org/obo/NCIT_C97073

http://linkedlifedata.com/resource/umls/id/C5680568

http://www.orpha.net/ORDO/Orphanet_183500

http://identifiers.org/medgen/1825988

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0002320

id

MONDO:0024237