genetic keratinization disorder associated with ocular features

Go to external page http://purl.obolibrary.org/obo/MONDO_0020267


This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:CN227842 (MONDO:equivalentTo)
  • Orphanet:98697 (MONDO:equivalentTo)
Subsets

ordo_group_of_disorders

exactMatch

http://linkedlifedata.com/resource/umls/id/CN227842

http://www.orpha.net/ORDO/Orphanet_98697

id

MONDO:0020267

Term relations