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Ontology Browser
Term:
autosomal dominant distal hereditary motor neuronopathy 5 (DOID:0111203)
Annotations: Rat: (4) Mouse: (4) Human: (5) Chinchilla: (4) Bonobo: (4) Dog: (4) Squirrel: (4) Pig: (4) Naked Mole-rat: (4) Green Monkey: (4)
Parent Terms Term With Siblings Child Terms
autosomal dominant distal hereditary motor neuronopathy 1  
autosomal dominant distal hereditary motor neuronopathy 10  
autosomal dominant distal hereditary motor neuronopathy 11  
autosomal dominant distal hereditary motor neuronopathy 12  
autosomal dominant distal hereditary motor neuronopathy 13  
autosomal dominant distal hereditary motor neuronopathy 14  
autosomal dominant distal hereditary motor neuronopathy 2  
autosomal dominant distal hereditary motor neuronopathy 3  
autosomal dominant distal hereditary motor neuronopathy 4  
autosomal dominant distal hereditary motor neuronopathy 5  
An autosomal dominant distal hereditary motor neuronopathy that is characterized by onset of distal muscle weakness and atrophy predominantly affecting the upper limbs in the first few decades of life and that has_material_basis_in heterozygous mutation in the GARS gene on chromosome 7p14. (DO)
autosomal dominant distal hereditary motor neuronopathy 6  
autosomal dominant distal hereditary motor neuronopathy 7  
autosomal dominant distal hereditary motor neuronopathy 8  
autosomal dominant distal hereditary motor neuronopathy 9  

Synonyms
Exact Synonyms: DHMN VA ;   DHMN5 ;   DHMN5A ;   DSMAV ;   DSMAVA ;   Dhmn-V ;   Distal Hereditary Motor Neuronopathy, Type V ;   Distal Hereditary Motor Neuropathy, Type V ;   Distal Spinal Muscular Atrophy, Type V ;   HMN 5A
Primary IDs: MESH:C563443
Alternate IDs: DOID:0111204 ;   MIM:600794
Xrefs: ORDO:139536
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/12690580 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/22703882 "DO" "DO"

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