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Monomelic amyotrophy

Orpha number ORPHA65684
Prevalence of rare diseases Unknown
Inheritance
  • Sporadic
Age of onset Adulthood
ICD 10 code
  • G12.8
MIM number
Synonym(s) Benign focal amyotrophy
Hirayama disease
Juvenile muscular atrophy of the distal upper limb

Summary


An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located on the right side of this page.




The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
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