Rare Zebra

Rare disease search prototype built on Orphanet data

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ORPHA:33577

Nodular non-suppurative panniculitis

Also called Idiopathic lobular panniculitis, Idiopathic nodular panniculitis, Pfeiffer-Weber-Christian syndrome, Relapsing febrile nodular nonsuppurative panniculitis, Relapsing febrile nodular panniculitis, WCD, Weber-Christian disease, Weber-Christian panniculitis

Body system
Skin diseases
Inheritance pattern
Not applicable
Typical age of onset
Adult
Estimated prevalence
Unknown (Worldwide)
Rarity class
Unknown

ORPHA:33577 is classified under "Skin diseases" in the Orphanet nomenclature.

Common signs

  • Edema
  • Subcutaneous nodule
  • Weight loss
  • Fever
  • Nausea and vomiting
  • Abdominal pain