Term info
database cross reference
- UMLS:CN227592 (MONDO:equivalentTo)
- Orphanet:79177 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
IAO 0000233
https://github.com/monarch-initiative/mondo/issues/4985
definition
An inherited metabolic disease that is has its basis in the disruption of gluconeogenesis.
exactMatch
http://linkedlifedata.com/resource/umls/id/CN227592, http://purl.obolibrary.org/obo/Orphanet_79177
has exact synonym
gluconeogenesis disorder, rare inborn error of gluconeogenesis, inborn error of gluconeogenesis, inborn gluconeogenesis disorder
id
MONDO:0019225