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Glutaric Acidemia Type 2
Glutaric acidemia type 2
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Inborn errors of metabolism
(106)
2-Methylbutyryl-CoA dehydrogenase deficiency
3 methylcrotonyl-coa carboxylase deficiency
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
Argininosuccinic acidemia
Beta-ketothiolase deficiency
Beta-ketothiolase deficiency
Carnitine uptake deficiency
Citrullinemia
D-Glyceric acidemia
Galactosemias
Glutaric acidemia type I
Glutaricaciduria I
Glycogenosis
Hypermethioninemia
Isobutyryl-CoA dehydrogenase deficiency
Isovaleric acidemia
LCHAD
Leukodystrophy, globoid cell
MCAD deficiency
Maple syrup urine disease
Methylmalonic acidemia
Newborn screening
PKU
Propionic acidemia
Trifunctional protein deficiency
Tyrosinemia
Tyrosinemia type II
Urea cycle disorders
Very-long-chain acyl-CoA dehydrogenase deficiency
2,4 Dienoyl-CoA reductase deficiency
3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Acatalasia
Acid lipase disease
Adenosine deaminase deficiency
Adenylosuccinate lyase deficiency
Aldolase A deficiency
Analbuminaemia
Arakawa's syndrome II
Argininemia
Aspartylgl- ucosaminuria
Carbamoyl phosphate synthetase I deficiency
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
Carnitine-- acylcarnitine translocase deficiency
Cholesteryl ester storage disease
Congenital disorder of glycosylation
Crigler-Najjar syndrome
DOOR syndrome
Dihydropyrimidine dehydrogenase deficiency
Disaccharidase
Essential fructosuria
Fucosidosis
Fumarase deficiency
Galactose-- 1-phosphate uridylyltransferase galactosemia
Glucose-galactose malabsorption
Glycogen storage disease type I
Glycogen storage disease type II
Glycogen storage disease type III
Glycogen storage disease type V
Guanidinoacetate methyltransferase deficiency
Hawkinsinuria
Hereditary fructose intolerance
Histidinemia
Holocarboxylase synthetase deficiency
Hyperlysinemia
Hyperprolinemia
Hypervalinemia
Idiosyncrasy
Inborn error of lipid metabolism
Inborn error of metabolism
Lecithin cholesterol acyltransferase deficiency
Lesch–Nyhan syndrome
Lipid storage disorder
Lipid storage disorders
Lysinuric protein intolerance
Lysosomal storage disease
Lysosomal storage diseases
Malonyl-CoA decarboxylase deficiency
Menkes disease
Metab-L
Methylmalonyl-CoA mutase deficiency
Mevalonate kinase deficiency
Myoadenylate deaminase deficiency
N-Acetylglutamate synthase deficiency
Niemann-Pick disease, type C
Ornithine transcarbamylase deficiency
Ornithine translocase deficiency
Prolidase deficiency
Pyruvate carboxylase deficiency
Pyruvate kinase deficiency
Refsum's disease
Rotor syndrome
Sarcosinemia
Schindler disease
Short-chain acyl-coenzyme A dehydrogenase deficiency
Sly syndrome
Smith-Lemli-Opitz syndrome
Succinic semialdehyde dehydrogenase deficiency
Tangier disease
Tetrahydrobiopterin deficiency
Trimethylaminuria
Type I tyrosinemia
Type III tyrosinemia
Urocanic aciduria
Wolman disease
X-linked ichthyosis
Zellweger syndrome
more...
Autosomal recessive disorders
(250)
2-Hydroxyglutaric aciduria
Biotinidase deficiency
Cerebrotendineous xanthomatosis
Congenital adrenal hyperplasia
Cystic fibrosis
Cystic fibrosis
Glanzmann thrombasthenia
Hartnup disease
Hb S
Homocystinuria
17-beta-hy- droxysteroid dehydrogenase deficiency
3 methylcrotonyl-coa carboxylase deficiency
Abdallat Davis Farrage syndrome
Abderhalde- n-Kaufmann-Lignac syndrome
Abetalipop- roteinemia
Ablepharon macrostomia syndrome
Acatalasia
Aceruloplasminemia
Acheiropodia
Acrocallosal syndrome
Acrodermatitis enteropathica
Acute fatty liver of pregnancy
Adducted thumb syndrome
Adenine phosphorib- osyltransferase deficiency
Adenosine deaminase deficiency
Adenylosuccinate lyase deficiency
Aicardi-Goutieres syndrome
Aldolase A deficiency
Alkaptonuria
Alpha-mannosidosis
Antley-Bixler syndrome
Argininemia
Argininosuccinic acidemia
Arterial tortuosity syndrome
Aspartylgl- ucosaminuria
Atelosteogenesis, type II
Atransferrinemia
Bare lymphocyte syndrome
Batten disease
Behr's syndrome
Bernard-Soulier syndrome
Beta-ketothiolase deficiency
Beta-mannosidosis
Bietti's crystalline dystrophy
Bloom syndrome
Blue diaper syndrome
CAMFAK syndrome
Canavan disease
Carbamoyl phosphate synthetase I deficiency
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
Carnitine uptake deficiency
Carnitine-- acylcarnitine translocase deficiency
Carnosinemia
Carpenter syndrome
Cartilage–hair hypoplasia
Cenani Lenz syndactylism
Chediak–Higashi syndrome
Chondrodystrophy
Chorea acanthocytosis
Citrullinemia
Cockayne syndrome
Compound heterozygosity
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Congenital hepatic fibrosis
Congenital ichthyosiform erythroderma
Congenital insensitivity to pain with anhidrosis
Craniodiaphyseal dysplasia
Cystathioninuria
Cystinosis
Cystinuria
D-Glyceric acidemia
DOOR syndrome
Diastrophic dysplasia
Dihydropyrimidine dehydrogenase deficiency
Donohue syndrome
Dubin-Johnson syndrome
Dubowitz syndrome
EAST syndrome
EEM syndrome
Ellis-van Creveld syndrome
Essential fructosuria
Ethylmalonic encephalopathy
Familial Mediterranean fever
Familial dysautonomia
Familial isolated vitamin E deficiency
Fanconi anemia
Farber disease
Fibrochondrogenesis
Finnish heritage disease
Fountain syndrome
Fraser syndrome
Friedreich's ataxia
Fucosidosis
Fumarase deficiency
GM2-gangliosidosis, AB variant
Galactokinase deficiency
Galactose epimerase deficiency
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galloway Mowat syndrome
Gangliosidosis
Gastroschisis
Gaucher's disease
Gerodermia osteodysplastica
Giant axonal neuropathy
Gitelman syndrome
Glucose-galactose malabsorption
Glutaric acidemia type I
Glutathione synthetase deficiency
Glycogen storage disease type I
Glycogen storage disease type II
Glycogen storage disease type III
Glycogen storage disease type V
Griscelli syndrome
Guanidinoacetate methyltransferase deficiency
Gunther disease
Harlequin type ichthyosis
Hemophagocytic lymphohistiocytosis
Hereditary pyropoikilocytosis
Hermansky–Pudlak syndrome
Histidinemia
Holocarboxylase synthetase deficiency
Hurler syndrome
Hyperlysinemia
Hypermethioninemia
Hyperprolinemia
Hypertryptophanemia
Hypervalinemia
ICF syndrome
Ichthyosis lamellaris
Iminoglycinuria
Impossible syndrome
Infantile free sialic acid storage disease
Infantile neuroaxonal dystrophy
Isobutyryl-CoA dehydrogenase deficiency
Isovaleric acidemia
Jervell and Lange-Nielsen syndrome
Johanson-Blizzard syndrome
Juvenile Primary Lateral Sclerosis
Kaufman oculocerebrofacial syndrome
Keutel syndrome
Kindler syndrome
LCHAD
Lafora disease
Laron syndrome
Lecithin cholesterol acyltransferase deficiency
Leukocyte adhesion deficiency
Leukodystrophy, globoid cell
Lipid storage disorder
Lipoid congenital adrenal hyperplasia
Lucey-Driscoll syndrome
Lysinuric protein intolerance
MCAD deficiency
Malonyl-CoA decarboxylase deficiency
Maple syrup urine disease
Meckel syndrome
Meleda disease
Metachromatic leukodystrophy
Methemoglobinemia
Methylmalonic acidemia
Mevalonate kinase deficiency
Micro syndrome
Microvillous inclusion disease
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
N-Acetylglutamate synthase deficiency
Nemaline myopathy
Nephronophthisis
Netherton syndrome
Neuronal ceroid lipofuscinosis
Nezelof syndrome
Niemann-Pick disease, type C
Niemann–Pick disease
Ochronosis
Oculodentodigital syndrome
Oguchi disease
Omenn syndrome
Ornithine translocase deficiency
Orotic aciduria
Otospondyl- omegaepiphyseal dysplasia
PKU
Papillon–Lefèvre syndrome
Pendred syndrome
Persistent Mullerian duct syndrome
Phosphofructokinase deficiency
Primary ciliary dyskinesia
Progressive external ophthalmoplegia
Prolidase deficiency
Propionic acidemia
Pseudodominance
Pseudoxanthoma elasticum
Purine nucleoside phosphorylase deficiency
Pycnodysostosis
Pyruvate carboxylase deficiency
Rabson-Mendenhall syndrome
Raine syndrome
Rapadilino syndrome
Recessive multiple epiphyseal dysplasia
Renal dysplasia-limb defects syndrome
Renal-hepa- tic-pancreatic dysplasia
Reproductive compensation
Restrictive dermopathy
Richner Hanhart syndrome
Rothmund–Thomson syndrome
Rotor syndrome
Sabinas brittle hair syndrome
Saccharopinuria
Salla disease
Sandhoff disease
Sanfilippo syndrome
Sarcosinemia
Short-chain acyl-coenzyme A dehydrogenase deficiency
Shwachman-Diamond syndrome
Sickle cell trait
Situs inversus
Sly syndrome
Smith-Lemli-Opitz syndrome
Succinic semialdehyde dehydrogenase deficiency
Sugarman syndrome
Survival motor neuron spinal muscular atrophy
Tangier disease
Tay-Sachs disease
Tetrahydrobiopterin deficiency
Thalassemia
Trifunctional protein deficiency
Trimethylaminuria
Triosephosphate isomerase deficiency
Type I tyrosinemia
Type III tyrosinemia
Tyrosinemia
Tyrosinemia type II
Urbach–Wiethe disease
Urocanic aciduria
Usher syndrome
Vaso-occlusive crisis
Very-long-chain acyl-CoA dehydrogenase deficiency
Vici syndrome
Weissenbac- her-Zweymüller syndrome
Werner syndrome
Wilson's disease
Wolcott-Rallison syndrome
Wolman disease
Woodhouse-Sakati syndrome
Xeroderma pigmentosum
Yunis-Varon syndrome
ZAP70 deficiency
Zazam Sheriff Phillips syndrome
Zunich–Kaye syndrome
more...
Genetic disorders
(40)
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Gangliosidoses gm2
Hereditary sensory and autonomic neuropathies
Nevoid basal cell carcinoma syndrome
Nevoid basal cell carcinoma syndrome
Glutaric acidemia type I
Isobutyryl-CoA dehydrogenase deficiency
Trifunctional protein deficiency
Leukodystrophy, globoid cell
3 methylcrotonyl-coa carboxylase deficiency
Very-long-chain acyl-CoA dehydrogenase deficiency
D-Glyceric acidemia
Carnitine uptake deficiency
Galactosemias
Cerebrotendineous xanthomatosis
Isovaleric acidemia
Methylmalonic acidemia
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
Glutaricaciduria I
PKU
Argininosuccinic acidemia
2-Methylbutyryl-CoA dehydrogenase deficiency
Maple syrup urine disease
LCHAD
Beta-ketothiolase deficiency
Tyrosinemia type II
Citrullinemia
MCAD deficiency
Hartnup disease
2-Hydroxyglutaric aciduria
Tyrosinemia
Glanzmann thrombasthenia
Biotinidase deficiency
Hypermethioninemia
Homocystinuria
Urea cycle disorders
Propionic acidemia
Hb S
Congenital adrenal hyperplasia
Cystic fibrosis
more...
Metabolic disorders
(60)
Albinism
Activated protein C resistance
Adenosine deaminase deficiency
Alcohol flush reaction
Antithrombin III deficiency
Antithrombin III deficiency
Baker IDI Heart and Diabetes Institute
Blue diaper syndrome
Childhood obesity
Congenital disorder of glycosylation
Congenital hyperinsulinism
Crigler-Najjar syndrome
Diagnostic fast
Disaccharidase
Disorders of calcium metabolism
Ectopic calcification
Farber disease
Fructose malabsorption
GM1 gangliosidoses
Galactosemias
Galactosemic cataract
Gangliosidoses gm2
Gangliosidosis
Gaucher's disease
Glycogen storage disease type 0
Hereditary fructose intolerance
Homocystinuria
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Hypoglycemia
Inborn errors of metabolism
Ketotic hypoglycemia
Lactose intolerance
Leukodystrophy, globoid cell
Lipid storage disorders
List of causes of hypoglycemia
Metab-L
Methemoglobinemia
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Obesity
Obesogen
Pickardt syndrome
Pycnodysostosis
Refeeding syndrome
Richner Hanhart syndrome
Rotor syndrome
Salicylate sensitivity
Schindler disease
Selfish Brain Theory
Sitosterolemia
Stress hyperglycemia
Sucrose intolerance
Tay-Sachs disease
Triosephosphate isomerase deficiency
Urbach–Wiethe disease
Urea cycle disorders
Winchester syndrome
Wolman disease
more...
Lysosomal storage diseases
Neuraminidase deficiency
Leukodystrophy, globoid cell
Gangliosidoses gm2
Pediatrics
Purpura, schoenlein-henoch
Congenital hypothyroidism
Hyperostosis, cortical, congenital
Inborn errors of metabolism
Newborn screening
Congenital adrenal hyperplasia
Cystic fibrosis
Autoimmune diseases
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Purpura, schoenlein-henoch
Diseases and disorders
(60)
Glossopharyngeal nerve diseases
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Physiologic nystagmus
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Inborn errors of renal tubular transport
Intervertebral disk displacement
Rosenthal syndrome
Brachial plexus neuropathies
Thiolase deficiency
Optic neuropathy, ischemic
Fatty acid oxidation disorders
Acidemia
Glutaric acidemia
Gastric cancer
Hyperammonemia
Hypotonia
Trifunctional protein deficiency
Leukodystrophy, globoid cell
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
D-Glyceric acidemia
Gangliosidoses gm2
Hereditary sensory and autonomic neuropathies
Metabolic disorders
Carnitine uptake deficiency
Galactosemias
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Cerebrotendineous xanthomatosis
Methylmalonic acidemia
Glutaricaciduria I
PKU
Giant cell glioblastoma
Argininosuccinic acidemia
Maple syrup urine disease
Neuraminidase deficiency
Beta-ketothiolase deficiency
Tyrosinemia type II
Citrullinemia
Hartnup disease
2-Hydroxyglutaric aciduria
Glycogenosis
Tyrosinemia
Glanzmann thrombasthenia
Biotinidase deficiency
Homocystinuria
Urea cycle disorders
Nevoid basal cell carcinoma syndrome
Hb S
Congenital hypothyroidism
Albinism
Dystonia
Congenital adrenal hyperplasia
Cystic fibrosis
more...
See also
(16)
Giant cell glioblastoma
L-3-hydroxyacyl CoA dehydrogenase
Acyl CoA dehydrogenase
Dehydrogenase
Glutaric acid
Glutaric acid
Autosomal recessive
Hearing test
Metabolism
Dystonia
Germ cell tumors
Amino acid metabolism
Flavoprotein
Medical genetics
Neil J. Gunther
Electron transfer
Neonatal
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