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Term:
3-Hydroxyacyl-CoA Dehydrogenase Deficiency
(DOID:9001715)
Annotations:
Rat: (3)
Mouse: (3)
Human: (4)
Chinchilla: (3)
Bonobo: (3)
Dog: (3)
Squirrel: (3)
Pig: (3)
Naked Mole-rat: (3)
Green Monkey: (3)
Parent Terms
Term With Siblings
Child Terms
inherited metabolic disorder
+
3-Hydroxyacyl-CoA Dehydrogenase Deficiency
3-methylglutaconic aciduria
+
5-Nucleotidase Syndrome
6-Phosphogluconolactonase Deficiency
aceruloplasminemia
Acetylcarnitine Deficiency
Acholinesterasemia
Acid Phosphatase Deficiency
Acute Reversible Leukoencephalopathy with Increased Urinary Alpha-ketoglutarate
Alpha-Fetoprotein Deficiency
Alpha-Fetoprotein, Hereditary Persistence of
amino acid metabolic disorder
+
Amino Acid Transport Disorders, Inborn
+
Angiotensin I-Converting Enzyme, Benign Serum Increase
Arene Oxide Detoxification Defect
aromatase excess syndrome
Aryl Hydrocarbon Hydroxylase Inducibility
bilirubin metabolic disorder
+
Butyrylcholinesterase Deficiency
Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type
carbohydrate metabolic disorder
+
CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO
Carnitine Acetyltransferase Deficiency
cerebral amyloid angiopathy
+
CHITOTRIOSIDASE DEFICIENCY
Chromate Resistance
Combined Congenital Deficiency of Intrinsic Factor and R Binder
Combined Defect of Growth Factors
Combined Exocrine Pancreatic Insufficiency
Combined Immunodeficiency and Megaloblastic Anemia with or without Hyperhomocysteinemia
congenital leptin deficiency
Congenital Nonspherocytic Hemolytic Anemia 4
Congenital Nonspherocytic Hemolytic Anemia 5
congenital secretory chloride diarrhea 1
congenital secretory sodium diarrhea 3
Copper Deficiency, Familial Benign
Coumarin Sensitivity
Deafness Hyperuricemia Neurologic Ataxia
Decreased Urinary Activity of Kallikrein
Defect in Hyaluronan Metabolism
Defect in Hydroxylation of Diphenylhydantoin
Deficient N-Hydroxylation of Amobarbital
Deoxyribose-5-Phosphate Aldolase Deficiency
dopamine beta-hydroxylase deficiency
DYSOSTOSIS MULTIPLEX, AIN-NAZ TYPE
Efavirenz, Poor Metabolism of
enterokinase deficiency
Ethanolaminosis
Familial Amyloidosis
+
familial erythrocytosis 8
familial hypocalciuric hypercalcemia
+
Familial Hypokalemia
+
FUCOSYLTRANSFERASE 6 DEFICIENCY
Glucocorticoid Receptor Deficiency
Glucose-Stimulated Secretory Diarrhea, with Common Variable Immunodeficiency
Glycoprotein Storage Disease
Glyoxalase II Deficiency
Gordon Holmes syndrome
Greenberg dysplasia
Hereditary Hyperbilirubinemia
+
Hypercalcemia, Infantile, 1
hyperphosphatemic familial tumoral calcinosis
+
Hypoadiponectinemia
immunodeficiency 43
immunoglobulin light chain amyloidosis
Inosine Triphosphatase Deficiency
isolated elevated serum creatine phosphokinase levels
isolated hyperchlorhidrosis
Lactate Dehydrogenase B Deficiency
Lactic Aciduria due to D-Lactic Acid
Leptin Receptor Deficiency
Leukotriene C4 Synthase Deficiency
lipid metabolism disorder
+
lysosomal storage disease
+
Malonic Aciduria
Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type
Mannose-Binding Protein Deficiency
Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency
Metabolic Brain Diseases, Inborn
+
metal metabolism disorder
+
Methemoglobin Reductase Deficiency
Methylmalonyl-Coenzyme A Mutase Deficiency
mitochondrial metabolism disease
+
Monocarboxylate Transporter 1 Deficiency
Monocyte Esterase Deficiency
Myeloperoxidase Deficiency
N Acetyltransferase Deficiency
+
neonatal diabetes mellitus with congenital hypothyroidism
Nonfunctional L-Gulonolactone Oxidase
overhydrated hereditary stomatocytosis
permanent neonatal diabetes mellitus
+
peroxisomal disease
+
Phenacetin O-Deethylase, Deficiency of
Phenol Sulfotransferase Deficiency
phosphoglycerate kinase 1 deficiency
Phosphohydroxylysinuria
plasma protein metabolism disease
+
Poor Drug Metabolism, CYP2C19-Related
Poor Drug Metabolism, CYP2D6-Related
Poor Metabolism of Proguanil
poor metabolism of thiopurines
+
porphyria
+
progeria
+
purine-pyrimidine metabolic disorder
+
pyrimidine metabolic disorder
+
renal tubular transport disease
+
Retinol-Binding Protein Deficiency
SEDOHEPTULOKINASE DEFICIENCY
sepiapterin reductase deficiency
Squalene Synthase Deficiency
steroid inherited metabolic disorder
+
Stomatocytosis II
Succinic Acidemia
SULFIDE:QUINONE OXIDOREDUCTASE DEFICIENCY
Thiamine Metabolism Dysfunction Syndrome 4 (Bilateral Striatal Degeneration and Progressive Polyneuropathy Type)
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type)
Thyrotropin-Releasing Hormone Deficiency
Transcobalamin I Deficiency
trimethylaminuria
Trypsinogen Deficiency
type 1 diabetes mellitus 2
Uridine-Cytidineuria
variant ABeta2M amyloidosis
vitamin metabolic disorder
+
warfarin resistance
warfarin sensitivity
+
Weinstein Kliman Scully Syndrome
Wiedemann Oldigs Oppermann Syndrome
Synonyms
Exact Synonyms:
3-Alpha-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency ; 3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency ; DEFICIENCY OF 3-HYDROXYACYL-COA DEHYDROGENASE ; HAD Deficiency ; HADH Deficiency ; HADHSC Deficiency ; L-3-Alpha-Hydroxyacyl-CoA Dehydrogenase, Short Chain, Deficiency ; M-SCHAD Deficiency ; SCHAD Deficiency
Primary IDs:
MESH:C535310
Alternate IDs:
MIM:231530