MeSH Treeview
Query OMIM entry list
606175
-
CARNITINE ACETYLTRANSFERASE DEFICIENCY
→
High-scoring List
Nervous System Diseases
Neurologic Manifestations
Dyskinesias
Ataxia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Database Center for Life Science