autosomal recessive distal spinal muscular atrophy 2 (Q16944450)

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human disease
  • distal hereditary motor neuropathy Jerash type
  • dHMNJ
  • spinal muscular atrophy Jerash type
  • DSMA2
  • Neuronopathy, Distal Hereditary Motor, Jerash Type
  • SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2
  • Autosomal recessive distal spinal muscular atrophy type 2
  • SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2
  • Spinal Muscular Atrophy, Distal, Autosomal Recessive, type 2
  • Spinal Muscular Atrophy, Jerash Type
  • Distal hereditary motor neuropathy, Jerash type
  • Neuropathy, Distal Hereditary Motor, Jerash Type
  • distal spinal muscular atrophy 2
  • Jerash type distal hereditary motor neuropathy
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Language Label Description Also known as
English
autosomal recessive distal spinal muscular atrophy 2
human disease
  • distal hereditary motor neuropathy Jerash type
  • dHMNJ
  • spinal muscular atrophy Jerash type
  • DSMA2
  • Neuronopathy, Distal Hereditary Motor, Jerash Type
  • SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2
  • Autosomal recessive distal spinal muscular atrophy type 2
  • SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2
  • Spinal Muscular Atrophy, Distal, Autosomal Recessive, type 2
  • Spinal Muscular Atrophy, Jerash Type
  • Distal hereditary motor neuropathy, Jerash type
  • Neuropathy, Distal Hereditary Motor, Jerash Type
  • distal spinal muscular atrophy 2
  • Jerash type distal hereditary motor neuropathy

Statements

instance of
rare disease
0 references
class of disease
0 references

Identifiers

Mondo ID
MONDO_0011585
0 references
 
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