JSON

[X] type 1 interferonopathy of childhood

Go to external page http://purl.obolibrary.org/obo/MONDO_0957408

A type 1 interferonopathy that occurs during childhood. [ MONDO:patterns/childhood ]

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C5681250 (MONDO:equivalentTo)
  • Orphanet:481671 (MONDO:equivalentTo)
  • GARD:21986 (MONDO:GARD)
  • MEDGEN:1843010 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, harrisons_view_connective_tissue_disorder, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, harrisons_view_syndromic_disease, mondo_top_grouping_connective_tissue_disorder, mondo_top_grouping_syndromic_disease, ordo_group_of_disorders

comment

This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'connective tissue disorder' (MONDO:0018153) ontology branch (https://orcid.org/0000-0002-1780-5230)

exactMatch

http://www.orpha.net/ORDO/Orphanet_481671

http://identifiers.org/medgen/1843010

http://linkedlifedata.com/resource/umls/id/C5681250

id

MONDO:0957408

term tracker item

https://github.com/monarch-initiative/mondo/issues/6878

https://github.com/monarch-initiative/mondo/issues/6742

https://github.com/monarch-initiative/mondo/issues/7365