obsolete distal hereditary motor neuronopathy type 2A

Term ID

DOID:0111208

Synonyms

• autosomal dominant adult spinal muscular atrophy IIA
• distal hereditary motor neuropathy type IIA
• HMN IIA
• HMN2A
• spinal Charcot-Marie-Tooth disease IIA

Definition

A distal hereditary motor neuropathy type 2 that has_material_basis_in heterozygous mutation in HSPB8 on 12q24.23. https://www.ncbi.nlm.nih.gov/pubmed/15122253

References

Obsolete

true

Secondary ID:

Merged into

autosomal dominant distal hereditary motor neuronopathy 2

Ontology

  ( DOID:0111208 )