neuronopathy, distal hereditary motor, autosomal recessive 5

Rare Disease

MONDO:0013947

Also known as:

DSMA5Young adult-onset dHMNautosomal recessive distal spinal muscular atrophy type 5

Young adult-onset distal hereditary motor neuropathy is a rare autosomal recessive distal hereditary motor neuropathy characterized by slowly progressive muscular weakness, hypotonia and atrophy of th...

Genes

Clinical Trials

–

Newborn Screening

–

Patient Groups

–

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

How we create this content →

Report Generation Failed

We couldn't automatically generate the report. This may be due to temporary service issues.

Companies Active in neuronopathy, distal hereditary motor, autosomal recessive 5

0 approved

Organizations with approved therapies for this disease

No approved therapies yet

Research is ongoing — 1 company has orphan drug designations for this disease

Servier Pharmaceuticals LLC

Other

Designated

View all companies active in neuronopathy, distal hereditary motor, autosomal recessive 5

Need this data in your product?

Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.

Explore API Start Free

← Back to All Diseases

neuronopathy, distal hereditary motor, autosomal recessive 5

Patient-Friendly Information

Companies Active in neuronopathy, distal hereditary motor, autosomal recessive 5

Need this data in your product?

Scientific Intelligence