familial Mediterranean fever, autosomal dominant
MONDO:0007601Mondo
Findings
No curated finding names familial Mediterranean fever, autosomal dominant yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Juvenile onset
HPO, annotations 2026-09-02
Features
11 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- ArthralgiaHPOHP:0002829
- 5 of 5 reported patients
- Polyarticular arthritisHPOHP:0005764
- 5 of 5 reported patients
- ProteinuriaHPOHP:0000093
- 5 of 5 reported patients
- Recurrent feverHPOHP:0001954
- 5 of 5 reported patients · Juvenile onset
- ErysipelasHPOHP:0001055
- 4 of 5 reported patients
- PleuritisHPOHP:0002102
- 4 of 5 reported patients
- Renal amyloidosisHPOHP:0001917
- 2 of 5 reported patients
- Renal insufficiencyHPOHP:0000083
- 2 of 5 reported patients
- Abdominal painHPOHP:0002027
- Chest painHPOHP:0100749
- PeritonitisHPOHP:0002586
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- MEFVHGNC:6998
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
Where it sits
- A kind of
Other names
1 name
Resolves to: familial Mediterranean fever, autosomal dominant
- Also called
- familial Mediterranean fever, AD