ORPHA:45
Adenosine monophosphate deaminase deficiency
Also called AMP deaminase deficiency, Myoadenylate deaminase deficiency
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- All ages
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:45 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.
Common signs
- Myalgia
- Muscle spasm
- Limb muscle weakness
- Exercise-induced myalgia
- Exercise-induced muscle fatigue