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Dictionary » 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:

Symptoms of 2M3HBA (Beta ketothiolase deficiency)

Some of the symptoms of 2M3HBA incude:

2M3HBA: Related Disease Topics

These medical disease topics may be related to 2M3HBA:

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

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  • Acromesomelic dwarfism campailla martinelli type
  • Acromesomelic dwarfism Maroteux type
  • Acromesomelic dysplasia
  • Acromesomelic dysplasia Brahimi Bacha type
  • Acromesomelic dysplasia Campailla Martinelli type
  • Acromesomelic dysplasia Hunter Thompson type
  • Acromesomelic dysplasia, Grebe type
  • Acromesomelic dysplasia, Maroteaux type
  • Acrometagenesis
  • Acrometageria
  • Acromial

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