2M3HBA

Introduction: 2M3HBA

Description of 2M3HBA

2M3HBA (medical condition): A rare inherited disease characterized by the bodies inability to metabolise...more »

See also:

Beta ketothiolase deficiency:
  »Introduction: Beta ketothiolase deficiency
  »Symptoms of Beta ketothiolase deficiency

2M3HBA as a Disease

2M3HBA: Another name for Beta ketothiolase deficiency (or close medical condition association).
  »Introduction: Beta ketothiolase deficiency
  »Symptoms of Beta ketothiolase deficiency

2M3HBA: Related Diseases

2M3HBA: 2M3HBA is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Metabolic conditions
• Congenital conditions - metabolic disorders
• Congenital conditions
• Mitochondrial conditions

Symptoms of 2M3HBA (Beta ketothiolase deficiency)

Some of the symptoms of 2M3HBA incude:

• Ketoacidic attacks
• Seizures
• High blood level of ammonia
• Psychomotor retardation
• Beta-ketothiolase deficiency

See full list of 9 symptoms of 2M3HBA (Beta ketothiolase deficiency)

2M3HBA: Related Disease Topics

These medical disease topics may be related to 2M3HBA:

• rare disorder
• autosomal recessive disorder
• vomiting
• dehydration
• coma
• ketoacidosis
• convulsions

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

More Medical Dictionary Topics

Acromial

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