3-Hydroxyacyl-Coa Dehydrogenase Deficiency (HADH DEFICIENCY)

Alias:
Deficiency of 3-Hydroxyacyl-Coa Dehydrogenase
Hadh Deficiency
3-Hydroxyacyl-Coenzyme a Dehydrogenase Deficiency
Schad Deficiency
Had Deficiency
L-3-Alpha-Hydroxyacyl-Coa Dehydrogenase, Short Chain, Deficiency
3-Alpha-Hydroxyacyl-Coenzyme a Dehydrogenase Deficiency
3-Alpha-Hydroxyacyl-Coa Dehydrogenase Deficiency
Hydroxyacyl-Coenzyme a Dehydrogenase Deficiency
Schad Deficiency, Formerly
M/schad Deficiency
Metabolic Diseases
Hadhsc Deficiency
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
3-Hydroxyacyl-Coa Dehydrogenase Deficiency, also known as deficiency of 3-hydroxyacyl-coa dehydrogenase, is related to long-chain 3-hydroxyacyl-coa dehydrogenase deficiency and hyperinsulinemic hypoglycemia, familial, 4, and has symptoms including emaciation An important gene associated with 3-Hydroxyacyl-Coa Dehydrogenase Deficiency is HADH (Hydroxyacyl-CoA Dehydrogenase). The drugs Elvitegravir and Methadone have been mentioned in the context of this disorder. Affiliated tissues include liver and skeletal muscle, and related phenotypes are hypotonia and feeding difficulties in infancy
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
9
6

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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References Literature

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