arthrogryposis multiplex congenita 7, X-linked
MONDO:0975826Mondo
Findings
No curated finding names arthrogryposis multiplex congenita 7, X-linked yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- X-linked inheritance
- Onset and course
- Second trimester onset
HPO, annotations 2026-09-02
Features
24 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.
- Anteverted naresHPOHP:0000463
- 2 of 2 reported patients
- Arthrogryposis multiplex congenitaHPOHP:0002804
- 3 of 3 reported patients
- Decreased fetal movementHPOHP:0001558
- 1 of 1 reported patient
- Depressed nasal bridgeHPOHP:0005280
- 2 of 2 reported patients
- Fetal hydrothoraxHPOHP:0025678
- 1 of 1 reported patient
- Fetal skin edemaHPOHP:0025672
- 2 of 2 reported patients
- Fixed elbow flexionHPOHP:0006471
- 1 of 1 reported patient
- Hand clenchingHPOHP:0001188
- 3 of 3 reported patients
- Hip flexion contractureHPOHP:0020025
- 1 of 1 reported patient
- Increased variability in muscle fiber diameterHPOHP:0003557
- 1 of 1 reported patient
- Knee extension contractureHPOHP:0034672
- 1 of 1 reported patient
- MacrocephalyHPOHP:0000256
- 1 of 1 reported patient
Show the remaining 12
- MicrognathiaHPOHP:0000347
- 2 of 2 reported patients
- Nonimmune hydrops fetalisHPOHP:0001790
- 1 of 1 reported patient
- PolyhydramniosHPOHP:0001561
- 1 of 1 reported patient
- Pulmonary hypoplasiaHPOHP:0002089
- 1 of 1 reported patient
- Rocker bottom footHPOHP:0001838
- 2 of 2 reported patients
- Short columellaHPOHP:0002000
- 1 of 1 reported patient
Where it sits
- A kind of