Diseases Associated With Branched-Chain Amino Acid Catabolic Process
Disease |
Maple Syrup Urine Disease
|
Liver Cirrhosis, Experimental
|
3-Methylcrotonyl Coa Carboxylase 2 Deficiency
|
3-Methylglutaconic Aciduria, Type I
|
Acidemia, Isovaleric
|
Lung Adenocarcinoma
|
Amino Acid Metabolism, Inborn Errors
|
Autism
|
Beta-Hydroxyisobutyryl Coa Deacylase Deficiency
|
Beta Ketothiolase Deficiency
|
Disease Progression
|
Hydroxyacyl-Coa Dehydrogenase, Type 2, Deficiency
|
Isobutyryl-Coa Dehydrogenase Deficiency
|
Kidney Failure, Chronic
|
Leigh Disease
|
Mental Retardation, X-Linked 17
|
Mental Retardation, X-Linked, Syndromic 10
|
Myocardial Ischemia
|
Obesity
|
Osteoarthritis
|
Precancerous Conditions
|
Seizures
|
Stomach Neoplasms
|
2-Methylbutyryl-Coa Dehydrogenase Deficiency
|
Weight Gain
|
3-Methylcrotonyl Coa Carboxylase 1 Deficiency
|