Rare Zebra

Rare disease search prototype built on Orphanet data

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ORPHA:168

Loose anagen syndrome

Body system
Skin diseases
Inheritance pattern
Autosomal dominant
Typical age of onset
Childhood
Estimated prevalence
Unknown (Worldwide)
Rarity class
Unknown

ORPHA:168 is classified under "Skin diseases" in the Orphanet nomenclature.

Common signs

  • Abnormality of the hair
  • Abnormal hair whorl
  • Iris coloboma