modern wellness · Condition
Carnitine Acetyltransferase Deficiency
phenotype · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Nutritional and Metabolic Diseases; Behavior and Behavior Mechanisms; Eye Diseases; Pathological Conditions, Signs and Symptoms
🏥 Names
Disease Name
Carnitine Acetyltransferase Deficiency
Alias Names / Synonyms
Carnitine Acetyltransferase Deficiency
Topic Type
phenotype
🧬 Ontology Classifications
DisGeNET Type
phenotype
UMLS Type
Disease or Syndrome
MeSH Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Nutritional and Metabolic Diseases; Behavior and Behavior Mechanisms; Eye Diseases; Pathological Conditions, Signs and Symptoms
🔗 External References