hadh Phenotypes

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Phenotypes

Gene Literature (2)

Nucleotides (325)

Interactants (67)

XB-GENEPAGE-1007277

Gene Symbol: hadh Gene Name: hydroxyacyl-CoA dehydrogenase

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (42 sources): Abnormal circulating acetylcarnitine concentration, Acute hepatic failure, Confusion, Decreased 3-hydroxyacyl-CoA dehydrogenase level, Decreased plasma carnitine, Diarrhea, Dicarboxylic aciduria, Dilated cardiomyopathy, Elevated circulating hepatic transaminase concentration, Failure to thrive, Fasting hyperinsulinemia, Feeding difficulties in infancy, Fulminant hepatic failure, Generalized hypotonia, Growth delay, Hepatic necrosis, Hepatic steatosis, Hyperammonemia, Hyperinsulinemic hypoglycemia, Hypertrophic cardiomyopathy, Hypoglycemic coma, Hypoglycemic encephalopathy, Hypoglycemic seizures, Hypoketotic hypoglycemia, Hypotonia, Increased C-peptide level, Increased circulating free fatty acid level, Intellectual disability, Intrauterine growth retardation, Lactic acidosis, Lethargy, Mildly elevated creatine kinase, Motor delay, Myoglobinuria, Neonatal hypoglycemia, Neonatal hypotonia, Peripheral neuropathy, Pigmentary retinopathy, Prolonged QT interval, Prolonged prothrombin time, Proportionate short stature, Vomiting [+]
Mouse (11 sources): abnormal fatty acid oxidation, abnormal fatty acids level, abnormal lipid homeostasis, abnormal pancreatic alpha cell morphology, decreased circulating glucose level, decreased circulating ketone body level, decreased respiratory quotient, decreased susceptibility to diet-induced obesity, increased body temperature, increased fatty acids level, increased insulin secretion [+]
View all ortholog results at Monarch