Disease

autosomal recessive distal hereditary motor neuronopathy 7

Definition

An autosomal recessive distal hereditary motor neuronopathy characterized by onset of lower leg weakness in the first decade and that has_material_basis_in homozygous or compound heterozygous mutation in the VWA1 gene on chromosome 1p36.

Synonyms

None

Cross References

MIM:619216

Parent Terms

autosomal recessive 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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