arthrogryposis multiplex congenita 6
MONDO:0030281Mondo
Findings
No curated finding names arthrogryposis multiplex congenita 6 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Death in infancy · Neonatal death · Death in childhood
HPO, annotations 2026-09-02
Features
10 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.
- AkinesiaHPOHP:0002304
- 5 of 5 reported patients
- Decreased fetal movementHPOHP:0001558
- 5 of 5 reported patients
- Nemaline bodiesHPOHP:0003798
- 5 of 5 reported patients
- Respiratory failureHPOHP:0002878
- 5 of 5 reported patients
- Arthrogryposis multiplex congenitaHPOHP:0002804
- 4 of 5 reported patients · Congenital onset
- PolyhydramniosHPOHP:0001561
- 3 of 4 reported patients · Fetal onset
- Adducted thumbHPOHP:0001181
- 1 of 5 reported patients
- Large fontanellesHPOHP:0000239
- 1 of 5 reported patients
- HypospadiasHPOHP:0000047
- Increased variability in muscle fiber diameterHPOHP:0003557
Where it sits
- A kind of
Other names
1 name
Resolves to: arthrogryposis multiplex congenita 6
- Also called
- AMC6