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Ontology Browser

Term:
multiple acyl-CoA dehydrogenase deficiency (DOID:0060358)
Annotations: Rat: (4) Mouse: (4) Human: (4) Chinchilla: (4) Bonobo: (4) Dog: (4) Squirrel: (4) Pig: (4)
Parent Terms Term With Siblings Child Terms
2-aminoadipic 2-oxoadipic aciduria  
2-hydroxyglutaric aciduria +   
2-Methylacetoacetyl CoA Thiolase Deficiency 
2-Methylbutyryl-CoA Dehydrogenase Deficiency  
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency  
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency  
3-Hydroxyisobutyric Aciduria 
5-Oxoprolinase Deficiency  
Adams Nance Syndrome 
adenine phosphoribosyltransferase deficiency  
adenylosuccinase lyase deficiency  
adult-onset ataxia and polyneuropathy  
Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 
Albinism +   
alkaptonuria +   
Alpha-Ketoglutarate Dehydrogenase Deficiency  
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis 
Aminoacylase 1 Deficiency  
Arakawa Syndrome 2 
argininosuccinic aciduria  
aromatic L-amino acid decarboxylase deficiency  
Asparagine Synthetase Deficiency  
Beta-Aminoisobutyric Acid, Urinary Excretion of  
Beta-Hydroxyisobutyryl CoA Deacylase Deficiency  
beta-ketothiolase deficiency  
BH4-deficient hyperphenylalaninemia A  
Bjornstad syndrome  
Blue Diaper Syndrome 
branched-chain keto acid dehydrogenase kinase deficiency  
Brunner syndrome  
Camptodactyly Taurinuria 
carbamoyl phosphate synthetase I deficiency disease  
carboxypeptidase N deficiency  
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal  
cerebral creatine deficiency syndrome +   
Childhood Myocerebrohepatopathy Spectrum  
coenzyme Q10 deficiency disease +   
combined oxidative phosphorylation deficiency +   
Cowden-Like Syndrome  
cystathioninuria  
Cysteine Peptiduria 
cystinuria +   
cytochrome-c oxidase deficiency disease +   
deafness-dystonia-optic neuronopathy syndrome  
Deoxyguanosine Kinase Deficiency  
developmental and epileptic encephalopathy 39  
Diaminopentanuria 
Dibasic Amino Aciduria I 
dicarboxylic aminoaciduria  
Dimethylglycine Dehydrogenase Deficiency  
Encephalopathy due to Defective Mitochondrial and Peroxisomal Fission +   
ethylmalonic encephalopathy  
Friedreich ataxia +   
fumarase deficiency  
GABA aminotransferase deficiency  
gamma-amino butyric acid metabolism disorder +   
gamma-glutamyl transpeptidase deficiency  
Global Developmental Delay, Progressive Ataxia, and Elevated Glutamine  
Glucoglycinuria  
Glutamate Monosodium Sensitivity 
glutamate-cysteine ligase deficiency  
Glutamine Deficiency, Congenital  
Glutaric Aciduria +   
glutathione synthetase deficiency +   
glycine encephalopathy +   
GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE  
Glycinuria with or without Oxalate Urolithiasis  
GRACILE syndrome  
Hartnup disease  
histidine metabolism disease +   
histidinemia  
homocystinuria +   
homocystinuria-megaloblastic anemia cblG type  
hydroxykynureninuria  
Hydroxyprolinemia 
hyperhomocysteinemia +   
Hyperleucine-Isoleucinemia 
hyperlysinemia +   
Hypermetabolism due to Defect in Mitochondria 
hypermethioninemia +   
hyperprolinemia +   
Hypertaurinuric Cardiomyopathy 
Hypertryptophanemia +   
hypomyelinating leukodystrophy 4  
hypotonia-cystinuria syndrome  
Ichthyosis, Split Hairs, and Amino Aciduria 
IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA  
Indolylacroyl Glycinuria with Mental Retardation 
Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development  
Isobutyryl-CoA Dehydrogenase Deficiency  
isolated sulfite oxidase deficiency  
isovaleric acidemia  
Ketoadipicaciduria 
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
Leber hereditary optic neuropathy +   
Leigh disease +   
leucine-sensitive hypoglycemia of infancy  
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation  
Lysine Malabsorption Syndrome 
lysinuric protein intolerance  
Maleylacetoacetate Isomerase Deficiency  
maple syrup urine disease +   
Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency 
Mercaptolactate-Cysteine Disulfiduria 
Methionine Malabsorption Syndrome 
Methylmalonate Semialdehyde Dehydrogenase Deficiency  
methylmalonic acidemia +   
Methylmalonyl-CoA Epimerase Deficiency +   
Mitochondrial Cardiomyopathy  
mitochondrial complex I deficiency +   
mitochondrial complex II deficiency +   
mitochondrial complex III deficiency +   
mitochondrial complex V (ATP synthase) deficiency +   
Mitochondrial Cytopathy +   
mitochondrial DNA depletion syndrome +   
mitochondrial DNA depletion syndrome 5  
Mitochondrial Phosphate Carrier Deficiency  
mitochondrial pyruvate carrier deficiency  
multiple acyl-CoA dehydrogenase deficiency +   
An inherited metabolic disorder characterized by the body's inability to break down proteins and fats to produce energy. It is a disorder of fatty acid, amino acid, and choline metabolism and has an autosomal recessive inheritance pattern. It has_material_basis_in mutations in the ETFA, ETFB and ETFDH genes. It presents three clinical phenotypes: a neonatal-onset form with congenital anomalies (type I), a neonatal-onset form without congenital anomalies (type II), and a late-onset form (type III). The neonatal-onset forms are usually fatal. (DO)
multiple carboxylase deficiency +   
multiple mitochondrial dysfunctions syndrome +   
Myopathy due to Malate-Aspartate Shuttle Defect 
Myopathy with Giant Abnormal Mitochondria 
Myopathy, Cataract, Hypogonadism Syndrome 
N-Acetylaspartate Deficiency  
Noninsulin-Dependent Diabetes Mellitus with Deafness  
nuclear type mitochondrial complex I deficiency 20  
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
optic atrophy 1  
organic acidemia +   
ornithine translocase deficiency  
Parkinson's Disease, Mitochondrial  
Pearson syndrome  
pentosuria  
phenylketonuria +   
Progressive External Ophthalmoplegia with Hypogonadism 
prolidase deficiency  
propionic acidemia +   
Proximal Myopathy with Focal Depletion of Mitochondria 
pyruvate carboxylase deficiency disease +   
pyruvate decarboxylase deficiency +   
Richards-Rundle Syndrome 
sarcosinemia  
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis  
serine deficiency +   
Spinocerebellar Ataxia with Epilepsy  
Succinate-Coa Ligase Deficiency +   
succinic semialdehyde dehydrogenase deficiency  
systemic primary carnitine deficiency disease  
Tiglic Acidemia 
Tryptophanuria with Dwarfism 
tyrosinemia +   
Tyrosinosis 
urea cycle disorder +   
Valinemia +   
VDAC Deficiency 
Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2  
very long chain acyl-CoA dehydrogenase deficiency  
Wolfram syndrome 2  

Synonyms
Exact Synonyms: ETFA Deficiencies ;   ETFB Deficiencies ;   ETFDH Deficiencies ;   Electron Transfer Flavoprotein Beta Subunit Deficiency ;   Electron Transfer Flavoprotein Deficiency ;   Electron Transfer Flavoprotein Dehydrogenase Deficiency ;   Ethylmalonic Adipic Aciduria ;   Ethylmalonic-Adipic Acidurias ;   GA II ;   GLUTARIC ACIDEMIA II ;   Glutaric Acidemia Type II ;   Glutaric Acidemia, Type 2 ;   Glutaric Aciduria II ;   Glutaric Aciduria IIA ;   Glutaric Aciduria IIB ;   Glutaric Aciduria IIC ;   Glutaric Aciduria Type 2 ;   Glutaric Aciduria Type II ;   MAD deficiency ;   MADD ;   MADD (Multiple Acyl CoA Dehydrogenase Deficiency) ;   MADDs (Multiple Acyl-CoA Dehydrogenase Deficiency) ;   electron transfer flavoprotein alpha subunit deficiency ;   electron transfer flavoprotein ubiquinone oxidoreductase deficiency ;   multiple FAD dehydrogenase deficiency
Narrow Synonyms: EMA GLUTARIC ACIDEMIA IIA ;   ETFA DEFICIENCY ;   ETFB DEFICIENCY ;   ETFDH DEFICIENCY ;   ETHYLMALONIC-ADIPICACIDURIA ;   GLUTARIC ACIDEMIA IIB ;   GLUTARIC ACIDEMIA IIC ;   GLUTARIC ACIDEMIA IIC, LATE-ONSET
Primary IDs: MESH:D054069
Alternate IDs: OMIM:231680
Xrefs: ICD10CM:E71.313 ;   NCI:C84907 ;   ORDO:26791
Definition Sources: http://ghr.nlm.nih.gov/condition/glutaric-acidemia-type-ii "DO", https://en.wikipedia.org/wiki/Glutaric_acidemia_type_2 "DO", https://www.ncbi.nlm.nih.gov/pubmed/12815589 "DO", https://www.ncbi.nlm.nih.gov/pubmed/22580358 "DO"

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