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

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/3492

exactMatch

http://identifiers.org/medgen/1826126

http://www.orpha.net/ORDO/Orphanet_96076

http://linkedlifedata.com/resource/umls/id/C5681581

id

MONDO:0019875