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inborn aminoacylase deficiency
Disease Summary
Associated Targets (3)
Tbio
3
Mondo Description An acquired metabolic disease that is has its basis in the disruption of aminoacylase activity.
Mondo Term and Equivalent IDs
MONDO:0017686: inborn aminoacylase deficiency
Orphanet:308448:
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
Orphanet:308448
MONDO:0017686
High level summary of knowledge for a disease, including descriptions and datasource references.