An inherited metabolic disease that is has its basis in the disruption of aminoacylase activity. [ MONDO : patterns/inborn_metabolic ]
This is just here as a test because I lose it
Term information
database
cross reference
- Orphanet:308448 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
conformsTo
- http://purl.obolibrary.org/obo/mondo/patterns/inborn_metabolic.yaml
- http://purl.obolibrary.org/obo/mondo/patterns/inborn_metabolic_disrupts.yaml
definition
- An inherited metabolic disease that is has its basis in the disruption of aminoacylase activity.
exactMatch
- http://www.orpha.net/ORDO/Orphanet_308448
has exact synonym
- inborn error of aminoacylase activity
- rare inborn error of aminoacylase activity
- inborn aminoacylase activity disorder
has related synonym
- aminoacylase deficiency
id
- MONDO:0017686
Term relations
Equivalent to:
Subclass of: