Glutaric Aciduria Iii (GA3)

Alias:
Glutaryl-Coa Oxidase Deficiency
Glutaric Acidemia Type 3
Glutaric Aciduria Type 3
Ga Iii
Ga3
Glutaric Aciduria 3
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Glutaric Aciduria Iii, also known as glutaryl-coa oxidase deficiency, is related to glutaric acidemia i and trichothiodystrophy, and has symptoms including diarrhea and vomiting. An important gene associated with Glutaric Aciduria Iii is SUGCT (Succinyl-CoA:Glutarate-CoA Transferase). Affiliated tissues include thymus and lymph node, and related phenotypes are glutaric aciduria and abnormality of circulating enzyme level
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
All ages
--
10
38
6

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Mutations
No data available

Related Drugs

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Phase
No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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IF
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