This is just here as a test because I lose it
Term information
database
cross reference
- Orphanet:101957 (MONDO:equivalentTo)
- GARD:19801 (MONDO:GARD)
- ICD10CM:E23.0 (Orphanet:101957/specific)
- icd11.foundation:292840069 (https://orcid.org/0000-0002-3458-4839)
Subsets
gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders