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Vasculopathy, Retinal, With Cerebral Leukodystrophy [Supplementary Concept]

mutations in TREX1

Date introduced: November 5, 2012

MeSH Unique ID: C566007

Heading Mapped to:

Entry Terms:

  • Retinopathy, Vascular, With Cerebral And Renal Involvement And Raynaud And Migraine Phenomena
  • Cerebroretinal Vasculopathy, Hereditary

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