ORPHA:85453
X-linked reticulate pigmentary disorder
Also called XLPDR, Familial cutaneous amyloidosis, PDR, Partington disease, X-linked cutaneous amyloidosis
- Body system
- Immunological diseases
- Inheritance pattern
- X-linked dominant
- Typical age of onset
- Childhood
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:85453 is classified under "Immunological diseases" in the Orphanet nomenclature.