methylcobalamin deficiency type cblE (Q55781940)

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human disease
  • HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblE COMPLEMENTATION TYPE
  • HMAE
  • Functional methionine synthase deficiency type cblE
  • Vitamin B12-Responsive Homocystinuria, Cble Type
  • Methylcobalamin Deficiency, Cble Type
  • HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblE COMPLEMENTATION TYPE; HMAE
  • Homocystinuria-Megaloblastic Anemia Due to Defect 1N Cobalamin Metabolism, Cble Complementation Type
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Language Label Description Also known as
English
methylcobalamin deficiency type cblE
human disease
  • HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblE COMPLEMENTATION TYPE
  • HMAE
  • Functional methionine synthase deficiency type cblE
  • Vitamin B12-Responsive Homocystinuria, Cble Type
  • Methylcobalamin Deficiency, Cble Type
  • HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblE COMPLEMENTATION TYPE; HMAE
  • Homocystinuria-Megaloblastic Anemia Due to Defect 1N Cobalamin Metabolism, Cble Complementation Type

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