robinow syndrome, autosomal recessive 2
Go to external page http://purl.obolibrary.org/obo/MONDO_0032800
This is just here as a test because I lose it
Term information
database
cross reference
- UMLS:C5193143 (MONDO:equivalentTo)
- OMIM:618529 (MONDO:equivalentTo)
- MEDGEN:1676687 (MONDO:equivalentTo)
Subsets
gard_rare, rare, nord_rare
exactMatch
http://identifiers.org/medgen/1676687
https://omim.org/entry/618529
http://linkedlifedata.com/resource/umls/id/C5193143