Arginine-Glycine Amidinotransferase Deficiency [Supplementary Concept]

mutation in GATM

Date introduced: November 5, 2012

MeSH Unique ID: C567192

Heading Mapped to:

• Amidinotransferases/deficiency
• Amino Acid Metabolism, Inborn Errors
• Developmental Disabilities
• Intellectual Disability
• Speech Disorders

Entry Terms:

• Arginine:Glycine Amidinotransferase Deficiency
• AGAT Deficiency
• Creatine Deficiency Syndrome due to AGAT Deficiency
• L-Arginine:Glycine Aminidotransferase Deficiency
• GATM Deficiency