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Peripheral amyelination

MedGen UID:
868208
Concept ID:
C4022600
Congenital Abnormality
HPO: HP:0030172

Definition

Congenital absence of the myelin sheath on a nerve. [from HPO]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVPeripheral amyelination

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