ORPHA:343
Hyperimmunoglobulinemia D with periodic fever
Also called HIDS, Hyper-IgD syndrome, Hyperimmunoglobinemia D with recurrent fever, Hyperimmunoglobulinemia D syndrome, Partial mevalonate kinase deficiency
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:343 is classified under "Immunological diseases" in the Orphanet nomenclature.
Common signs
- Recurrent fever
- Abdominal pain
- Gastrointestinal hemorrhage
- Hepatomegaly
- Lymphadenopathy
- Arthralgia