Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD)

Alias:
Gamma-Hydroxybutyric Aciduria
4-Hydroxybutyric Aciduria
Ssadh Deficiency
Succinate-Semialdehyde Dehydrogenase Deficiency
Gaba Metabolic Defect
Ssadhd
Ssadh
Deficiency, Succinate-Semialdehyde Dehydrogenase
Succinate Semialdehyde Dehydrogenase Deficiency
Gamma-Hydroxybutyric Acidemia
4-Hydroxybutyricaciduria
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Succinic Semialdehyde Dehydrogenase Deficiency, also known as gamma-hydroxybutyric aciduria, is related to gaba-transaminase deficiency and gaba aminotransferase deficiency, and has symptoms including ataxia, seizures and absence seizures. An important gene associated with Succinic Semialdehyde Dehydrogenase Deficiency is ALDH5A1 (Aldehyde Dehydrogenase 5 Family Member A1), and among its related pathways/superpathways are Metabolism and Regulation of expression of SLITs and ROBOs. The drugs SGS-742 and Neuroprotective Agents have been mentioned in the context of this disorder. Affiliated tissues include eye and brain, and related phenotypes are intellectual disability and ataxia
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
--
25
164
97

Medical Symptom

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Gene & Mutation

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References Literature

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