Rheumatology · Rheumatology / Autoinflammatory disease
Hyper-IgD syndrome
also: HIDS; Mevalonate kinase deficiency
Recurrent fever with lymphadenopathy and elevated IgD.
- Specialty
- Rheumatology
- Subspecialty
- Rheumatology / Autoinflammatory disease
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes, infancy
- Gene(s) involved
- MVK
- Alternative names & eponyms
- HIDS; Mevalonate kinase deficiency
Etiology & mechanism
Deficiency of mevalonate kinase.
Gene(s) involved (1)
Symptoms & signs (7)
In plain terms, someone with Hyper-IgD syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
2 shared
Blind loop syndrome
abdominal pain, diarrhea
2 shared
Carcinoid syndrome
abdominal pain, diarrhea
2 shared
Henoch–Schönlein purpura syndrome
abdominal pain, arthralgia
2 shared
Irritable bowel syndrome
abdominal pain, diarrhea
2 shared
Juvenile polyposis syndrome
abdominal pain, diarrhea
2 shared
Kawasaki syndrome
cervical lymphadenopathy, rash
2 shared
Multisystem inflammatory syndrome in children
abdominal pain, rash
1 shared
Acquired immunodeficiency syndrome
diarrhea
1 shared
Acute fatty liver of pregnancy syndrome
abdominal pain
1 shared
Alpha-gal syndrome
abdominal pain
Shares genes with
None.
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