Maple Syrup Urine Disease (MSUD)

Alias:
Bckd Deficiency
Msud
Branched-Chain Ketoaciduria
Branched-Chain Alpha-Keto Acid Dehydrogenase Deficiency
Intermittent Maple Syrup Urine Disease
Maple Syrup Urine Disease, Type Ii
Classic Maple Syrup Urine Disease
Branched-Chain 2-Ketoacid Dehydrogenase Deficiency
Thiamine-Responsive Maple Syrup Urine Disease
Intermediate Maple Syrup Urine Disease
Keto Acid Decarboxylase Deficiency
Maple Syrup Urine Disease, Type Ia
Maple Syrup Urine Disease Type 1a
Maple Syrup Urine Disease Type 1b
Maple Syrup Urine Disease Type 2
Branched Chain Ketoaciduria
Bckdh Deficiency
Ketoacidaemia
Thiamine-Responsive Branched-Chain Alpha-Ketoacid Dehydrogenase Deficiency
Intermittent Branched-Chain Alpha-Ketoacid Dehydrogenase Deficiency
Bckd - [branched-Chain Alpha-Ketoacid Dehydrogenase Deficiency]
Classic Branched-Chain Alpha-Ketoacid Dehydrogenase Deficiency
Lactic Acidosis, Congenital Infantile, Due to Lad Deficiency
Branched-Chain Ketoacid Dehydrogenase Deficiency
Branched Chain Ketoacid Dehydrogenase Deficiency
Dihydrolipoamide Dehydrogenase Deficiency
Nadh Cytochrome B5 Reductase Deficiency
Classic Branched-Chain Ketoaciduria
Thiamine-Responsive Bckd Deficiency
Maple Syrup Urine Disease, Type Ib
Maple Syrup Urine Disease, Type 1b
Msud - [maple-Syrup-Urine Disease]
Maple Syrup Urine Disease Type Ia
Maple Syrup Urine Disease Type Ib
Maple Syrup Urine Disease Type Ii
Ketoacid Decarboxylase Deficiency
Oxoacid Decarboxylase Deficiency
Intermittent Bckd Deficiency
Maple Syrup Urine Disease 1a
Maple Syrup Urine Disease 1b
Maple Syrup Urine Disease 2
Maple-Syrup-Urine Disorder
Maple-Syrup-Urine Syndrome
Thiamine-Responsive Msud
Classic Bckd Deficiency
Maple Syrup Disease
Ketoaminoacidaemia
Intermittent Msud
Ketoacidemia
Classic Msud
Msud Type Ia
Msud Type Ib
Msud Type Ii
Ketonemia
Msud1a
Msud1b
Msud2
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Maple Syrup Urine Disease, also known as bckd deficiency, is related to dihydrolipoamide dehydrogenase deficiency and intermediate maple syrup urine disease, and has symptoms including ataxia, lethargy and seizures. An important gene associated with Maple Syrup Urine Disease is BCKDHA (Branched Chain Keto Acid Dehydrogenase E1 Subunit Alpha), and among its related pathways/superpathways are Metabolism and Regulation of expression of SLITs and ROBOs. The drugs Dapagliflozin and Enzyme Inhibitors have been mentioned in the context of this disorder. Affiliated tissues include brain and heart, and related phenotypes are intellectual disability and seizure
Related ID:
MESH:D008375
ICD11:1623706568

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
1-9/100000
40
229
218

Medical Symptom

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

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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