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3-methylglutaconic aciduria type 9

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal recessive disease characterized by early-onset seizures, severely delayed psychomotor development and intellectual disability. Patients have hypotonia or spasticity, and laboratory investigations show increased serum lactate and 3-methylglutaconic aciduria.
Mondo Term and Equivalent IDs
MONDO:0044724:  3-methylglutaconic aciduria type 9
Orphanet:505216: 
UMLS:CN510468: