acadm Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (401)

Interactants (14)

XB-GENEPAGE-972934

Gene Symbol: acadm Gene Name: acyl-CoA dehydrogenase medium chain

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (45 sources): Abnormal circulating lactate dehydrogenase concentration, Arrhythmia, Ataxia, Bilateral tonic-clonic seizure, Cachexia, Cardiomegaly, Cerebral edema, Coma, Decreased liver function, Decreased plasma carnitine, Decreased plasma total carnitine, Delayed speech and language development, Diarrhea, Dicarboxylic aciduria, Distal arthrogryposis, Elevated circulating creatine kinase concentration, Elevated circulating hepatic transaminase concentration, Elevated urinary 3-hydroxybutyric acid, Exercise-induced myalgia, Exertional dyspnea, Fatigable weakness, Fatigable weakness of neck muscles, Fatigue, Febrile seizure (within the age range of 3 months to 6 years), Generalized hypotonia, Global developmental delay, Hepatic steatosis, Hepatomegaly, Hyperammonemia, Hyperglycinuria, Hypoglycemia, Hypotonia, Ketosis, Lethargy, Loss of consciousness, Macrocephaly, Medium chain dicarboxylic aciduria, Metabolic acidosis, Muscle spasm, Myopathy, Proximal muscle weakness, Reduced tendon reflexes, Seizure, Skeletal muscle atrophy, Vomiting [+]
Mouse (12 sources): abnormal aorta elastic tissue morphology, abnormal blood homeostasis, abnormal myocardial fiber morphology, abnormal vibrissa morphology, cardiac fibrosis, decreased circulating glucose level, impaired adaptive thermogenesis, increased circulating carnitine level, macrovesicular hepatic steatosis, microvesicular hepatic steatosis, myocardial fiber degeneration, postnatal lethality, incomplete penetrance [+]
View all ortholog results at Monarch