Rare Zebra

Rare disease search prototype built on Orphanet data

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ORPHA:377

Gorlin syndrome

Also called Basal cell nevus syndrome, Gorlin-Goltz syndrome, NBCCS, Nevoid basal cell carcinoma syndrome

Body system
Skin diseases
Inheritance pattern
Autosomal dominant
Typical age of onset
Adolescent, Adult
Estimated prevalence
1-9 / 100 000 (Europe)
Rarity class
1-9 / 100 000

ORPHA:377 is classified under "Skin diseases" in the Orphanet nomenclature.

Common signs

  • Neoplasm
  • Palmar pits
  • Plantar pits
  • Melanocytic nevus
  • Cerebral calcification
  • Macrocephaly