Guanidinoacetate methyltransferase deficiency

MONDO:0012999

A creatine deficiency syndrome characterized by global developmental delay/intellectual disability (DD/ID), prominent speech delay, autistic/hyperactive behavioral disorders, seizures, and various types of pyramidal and/or extra-pyramidal manifestations.

Also known as: GAMT deficiency, cerebral creatine deficiency syndrome 2, cerebral creatine deficiency syndrome type 2, disorder of guanidinoacetate N-methyltransferase activity, guanidinoacetate N-methyltransferase activity disease, guanidinoacetate methyltransferase deficiency, CCDS2, creatine deficiency syndrome due to GAMT deficiency

25 clinical trials for this condition and its sub-types.

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