congenital disorder of glycosylation, type Iw, autosomal dominant
Go to external page http://purl.obolibrary.org/obo/MONDO_0859223
This is just here as a test because I lose it
Term information
database
cross reference
- MEDGEN:1794278 (MONDO:equivalentTo)
- OMIM:619714 (MONDO:equivalentTo)
- UMLS:C5562068 (MONDO:equivalentTo)
Subsets
gard_rare, rare
exactMatch
https://omim.org/entry/619714
http://linkedlifedata.com/resource/umls/id/C5562068
http://identifiers.org/medgen/1794278