inborn disorder of phenylalanine and tyrosine metabolism
http://purl.obolibrary.org/obo/MONDO_0019235
Term info
database cross reference
- UMLS:CN227599 (MONDO:equivalentTo)
- Orphanet:79190 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
IAO 0000233
https://github.com/monarch-initiative/mondo/issues/4985
exactMatch
http://purl.obolibrary.org/obo/Orphanet_79190, http://linkedlifedata.com/resource/umls/id/CN227599
excluded subClassOf
http://purl.obolibrary.org/obo/MONDO_0019189
has exact synonym
inborn disorder of phenylalanin or tyrosine metabolism
has related synonym
disorder of phenylalanin or tyrosine metabolism
id
MONDO:0019235