Carnitine Palmitoyltransferase Ii Deficiency, Infantile

Nume		Carnitine Palmitoyltransferase Ii Deficiency, Infantile
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10		Disorders of fatty-acid metabolism
Clasificare anatomică Malacards		Boli hepatice; Boli neuronale

Boli A-Z		3-Hydroxyacyl-Coa Dehydrogenase Deficiency Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia Neuropathy Spectrum Blood Group--Ahonen Blood Group, I System Carnitine-Acylcarnitine Translocase Deficiency Carnitine Deficiency, Systemic Primary Carnitine Palmitoyltransferase I Deficiency Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal Crouzon Syndrome Dandy-Walker Syndrome Dilated Cardiomyopathy Hepatitis Holocarboxylase Synthetase Deficiency Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoglycemia Lipid Metabolism Disorder Malignant Hyperthermia Metabolic Acidosis Multiple Acyl-Coa Dehydrogenase Deficiency Myoglobinuria Myoglobinuria, Acute Recurrent, Autosomal Recessive Myoglobinuria, Recurrent Pancreatitis Visceral Steatosis