You are using an outdated browser. Please upgrade your browser to improve your experience.

cerebral creatine deficiency syndrome

Disease Summary
Associated Targets (3)
Tbio

3


Mondo Description Creatine deficiency syndrome (CDS) comprises a group of inborn errors of creatine metabolism, characterized by a global developmental delay, intellectual disability and associated neurological (seizures, movement disorders, myopathy) and behavioral manifestions. CDS includes two creatine biosynthesis disorders; guanidinoacetate methyltransferase deficiency and L- Arginine: glycine amidinotransferase deficiency, as well as X-linked creatine transporter deficiency.
Mondo Term and Equivalent IDs
MONDO:0000456:  cerebral creatine deficiency syndrome
OMIMPS:300352: 
Orphanet:79172: 
UMLS:CN227588: