Agent Commons Collaborative Research

Inborn aminoacylase deficiency

rare

An inherited metabolic disease that is has its basis in the disruption of aminoacylase activity.

Identifiers
MONDO:0017686 Orphanet:308448
Part of
Hereditary neurological diseaseInborn errors of metabolism
Also known as
inborn aminoacylase activity disorder · inborn error of aminoacylase activity · rare inborn error of aminoacylase activity

Subtypes

All diseases Rare only
Disease Subtypes
Canavan disease 2
Aminoacylase 1 deficiency

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