JSON

[X] Huntington disease-like syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0015548

Synonyms: Huntington disease phenocopy syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:C580174 (MONDO:equivalentTo)
  • Orphanet:158266 (MONDO:equivalentTo)
  • MEDGEN:777988 (MONDO:equivalentTo)
  • ICD9:333.99 (MONDO:relatedTo)
  • UMLS:C3711380 (MONDO:equivalentTo)
  • SCTID:702376003 (MONDO:equivalentTo)
  • GARD:20029 (MONDO:GARD)
Subsets

matrix_llm__is_cancer_other, gard_rare, disease_grouping, matrix_llm__txgnn_other, mondo_top_grouping_member, harrisons_view_psychiatric_disorder, matrix_txgnn_grouping_member, rare, matrix_txgnn_grouping_psychiatric_disorder, harrisons_view_nervous_system_disorder, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, 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, mondo_top_grouping_psychiatric_disorder, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease, ordo_group_of_disorders

exactMatch

http://linkedlifedata.com/resource/umls/id/C3711380

http://identifiers.org/mesh/C580174

http://identifiers.org/snomedct/702376003

http://identifiers.org/medgen/777988

http://www.orpha.net/ORDO/Orphanet_158266

id

MONDO:0015548