Search Ontology:
Human Disease

autosomal dominant distal hereditary motor neuronopathy 2

Term ID
DOID:0111206
Synonyms
  • distal hereditary motor neuronopathy type 2
  • distal hereditary motor neuronopathy type 2A
  • distal hereditary motor neuropathy type II
  • HMN II
  • HMN2
Definition
An autosomal dominant distal hereditary motor neuronopathy that is characterized by onset of slowly progressive distal limb weakness and atrophy between the second and fifth decades of life. (2)
References
Ontology
Human Disease   ( DOID:0111206 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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