Juvenile dermatomyositis (JDM) is the early-onset form of dermatomyositis (DM), a systemic, autoimmune inflammatory muscle disorder, characterized by proximal muscle weakness, evocative skin lesion, and systemic manifestations. [ Orphanet:93672 ]
Synonyms: myoseptumitis juvenile DM childhood dermatomyositis myoseptum inflammation inflammation of myoseptum juvenile dermatomyositis
Term information
- EFO:0000557 (MONDO:equivalentTo)
- MESH:C538250 (Orphanet:93672/e)
- NANDO:2200418 (https://orcid.org/0000-0003-0011-764X)
- SCTID:1212005 (MONDO:equivalentTo)
- icd11.foundation:1428089375 (Orphanet:93672)
- UMLS:C0263666 (MONDO:equivalentTo)
- MedDRA:10008521 (Orphanet:93672/e)
- GARD:6805 (MONDO:GARD)
- MESH:C000598745 (MONDO:equivalentObsolete)
- Orphanet:93672 (MONDO:equivalentTo)
- MEDGEN:120486 (MONDO:equivalentTo)
- DOID:14203 (MONDO:equivalentTo)
- NCIT:C27576 (MONDO:equivalentTo)
gard_rare, ordo_disorder, matrix_llm__is_cancer_other, mondo_top_grouping_idiopathic_disease, harrisons_view_connective_tissue_disorder, mondo_top_grouping_integumentary_system_disorder, mondo_top_grouping_member, matrix_llm__txgnn_other, nord_rare, matrix_included, harrisons_view_inflammatory_disease, rare, mondo_top_grouping_inflammatory_disease, harrisons_view_musculoskeletal_system_disorder, orphanet_rare, harrisons_view_integumentary_system_disorder, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, mondo_top_grouping_connective_tissue_disorder
http://purl.obolibrary.org/obo/mondo/patterns/specific_inflammatory_disease_by_site.yaml
http://purl.obolibrary.org/obo/mondo/patterns/inflammatory_disease_by_site.yaml
http://purl.obolibrary.org/obo/mondo/patterns/specific_infectious_disease_by_location.yaml
http://purl.obolibrary.org/obo/NCIT_C27576
http://identifiers.org/snomedct/1212005
http://identifiers.org/medgen/120486
http://linkedlifedata.com/resource/umls/id/C0263666
http://www.ebi.ac.uk/efo/EFO_0000557
http://www.orpha.net/ORDO/Orphanet_93672
http://purl.obolibrary.org/obo/DOID_14203
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1428089375
JDM
juvenile myositis
myopathy, familial idiopathic inflammatory
JPM
myositis
childhood type dermatomyositis