JSON

[X] progressive muscular dystrophy

Go to external page http://purl.obolibrary.org/obo/MONDO_0016106

Synonyms: progressive muscular dystrophy

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C4551827 (MONDO:equivalentTo)
  • MEDGEN:1633060 (MONDO:equivalentTo)
  • Orphanet:206644 (MONDO:equivalentTo)
  • GARD:20360 (MONDO:GARD)
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, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, clingen, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease, harrisons_view_musculoskeletal_system_disorder, ordo_group_of_disorders, harrisons_view_nervous_system_disorder

ClinGen label
progressive muscular dystrophy [ Orphanet:206644 ]

contributor

https://orcid.org/0000-0002-4142-7153

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

curated content resource

https://search.clinicalgenome.org/kb/conditions/MONDO:0016106

exactMatch

http://linkedlifedata.com/resource/umls/id/C4551827

http://identifiers.org/medgen/1633060

http://www.orpha.net/ORDO/Orphanet_206644

id

MONDO:0016106

Term relations

Subclass of: