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Hypoplastic pilosebaceous units

MedGen UID:
Concept ID:
HPO: HP:0007515

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVHypoplastic pilosebaceous units

Conditions with this feature

Ectodermal dysplasia with natal teeth, Turnpenny type
MedGen UID:
Concept ID:
Disease or Syndrome
A rare disorder with manifestation of hypo or oligodontia and acanthosis nigricans. It has been described in four generations of one family. Onset generally occurs during adolescence. Some patients are born with multiple teeth. Hair anomalies (sparse body and scalp hair) also reported. Inheritance is autosomal dominant.

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