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Constitutional megaloblastic anemia with severe neurologic disease

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ORPHA:319651

Classification level: Disorder

Synonym(s):
  • DHFR deficiency
  • Dihydrofolate reductase deficiency

Prevalence: <1 / 1 000 000

Inheritance: -

Age of onset: Childhood, Infancy

ICD-10: D52.8

ICD-11: 3A02.Y

OMIM: 613839

UMLS: C3151205

MeSH: C565095

GARD: 11000

Summary

An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page.

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