Disease

autosomal dominant distal hereditary motor neuronopathy 2

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.

Synonyms

autosomal dominant adult spinal muscular atrophy IIA
distal hereditary motor neuronopathy type 2

Cross References

Parent Terms

autosomal dominant distal hereditary motor neuronopathy

Child Terms

None

Sources of Associations

Associated Genes

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Associated Alleles

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Associated Models

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