Beckwith-Wiedemann syndrome due to 11p15 microduplication
Go to external page http://purl.obolibrary.org/obo/MONDO_0019875
This is just here as a test because I lose it
Term information
database
cross reference
- UMLS:C5681581 (MONDO:equivalentTo)
- GARD:19308 (MONDO:GARD)
- MEDGEN:1826126 (MONDO:equivalentTo)
- Orphanet:96076 (MONDO:equivalentTo)
Subsets
gard_rare, rare, ordo_subtype_of_a_disorder, nord_rare, ordo_etiological_subtype
exactMatch
http://identifiers.org/medgen/1826126
http://www.orpha.net/ORDO/Orphanet_96076
http://linkedlifedata.com/resource/umls/id/C5681581