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Methylcobalamin deficiency type cblG

ORPHA:2170

Classification level: Subtype of disorder
  • Synonym(s):
    • Functional methionine synthase deficiency type cblG
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: All ages
  • ICD-10: E72.1
  • OMIM: 250940
  • UMLS: C1855128
  • MeSH: -
  • GARD: 3577
  • MedDRA: -

Summary

This disease is described under Homocystinuria without methylmalonic aciduria

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