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disorder of methionine catabolism

Go to external page http://purl.obolibrary.org/obo/MONDO_0000351

An inherited metabolic disease that is has its basis in the disruption of methionine catabolic process. [ MONDO:patterns/inborn_metabolic ]

Synonyms: hypermethioninemia inborn methionine catabolic process disorder rare inborn error of methionine catabolic process inborn error of methionine catabolic process

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C4048705 (MONDO:equivalentTo)
  • HP:0003235 (MONDO:otherHierarchy)
  • SCTID:43123004 (MONDO:equivalentTo)
  • DOID:0050544 (MONDO:equivalentTo)
Subsets

rare, inferred_rare

exactMatch

http://purl.obolibrary.org/obo/DOID_0050544

http://identifiers.org/snomedct/43123004

http://linkedlifedata.com/resource/umls/id/C4048705

id

MONDO:0000351