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Autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature

MedGen UID:
1842650
Concept ID:
C5679967
Disease or Syndrome
Synonym: Autosomal dominant disease associated with punctate palmoplantar hyperkeratosis as a major feature
 
Orphanet: ORPHA308031

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVAutosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature

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