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| Term | autosomal recessive distal hereditary motor neuronopathy 3 | ID (Ontology) | DOID:0111211 (Human Disease) |
| Definition | An autosomal recessive distal hereditary motor neuronopathy characterized by juvenile onset of distal muscle weakness and wasting with variable severity that has_material_basis_in homozygous mutation in a 2.6-cM region of chromosome 11q13.3. | ||
| Also Known As | "autosomal recessive distal spinal muscular atrophy type 3" ; "dHMN3" ; "dHMN3 and dHMN4" (for all, see Synonyms field below) | ||
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autosomal recessive disease__ spinal muscular atrophy______| autosomal recessive distal hereditary motor neuronopathy |__autosomal recessive distal hereditary motor neuronopathy 3 |
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| Is a | autosomal recessive distal hereditary motor neuronopathy | ||
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MESH:C564626 MIM:607088 ORDO:139547 SNOMEDCT_US_2023_03_01:770430000 UMLS_CUI:C1846823 |
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