Farber disease
Engelsk navn: Farber disease
Engelske synonym: Acid ceramidase deficiency,Farber lipogranulomatosis
Definisjon
A subcutaneous tissue disease characterized by a spectrum of clinical signs ranging from the classical triad of painful and progressively deformed joints, subcutaneous nodules, and progressive hoarseness (due to laryngeal involvement) that presents in infancy, to varying phenotypes with respiratory and neurologic involvement.
Fra Orphanet
ORPHA: 333
Klassifiseringsnivå: Disorder
ICD-10: E75.2
Mer informasjon
Deler av informasjonen over er hentet fra ORPHAdata med lisens: Commons Attribution 4.0 International (CC BY 4.0)
