mosaic variegated aneuploidy syndrome 3
MONDO:0054736Mondo
Findings
No curated finding names mosaic variegated aneuploidy syndrome 3 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
- Infantile onset · Childhood onset
HPO, annotations 2026-09-02
Features
16 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.
- NephroblastomaHPOHP:0002667
- 6 of 6 reported patients
- Premature chromatid separationHPOHP:0200024
- 3 of 3 reported patients
- Short statureHPOHP:0004322
- 1 of 1 reported patient
- MicrocephalyHPOHP:0000252
- 3 of 6 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 6 reported patients
- Growth delayHPOHP:0001510
- 2 of 6 reported patients
- Arthrogryposis multiplex congenitaHPOHP:0002804
- 1 of 6 reported patients
- Cleft palateHPOHP:0000175
- 1 of 6 reported patients
- Convex nasal ridgeHPOHP:0000444
- 1 of 6 reported patients
- Deeply set eyeHPOHP:0000490
- 1 of 6 reported patients
- Few cafe-au-lait spotsHPOHP:0007429
- 1 of 6 reported patients
- Horseshoe kidneyHPOHP:0000085
- 1 of 6 reported patients
Show the remaining 4
- Low-set earsHPOHP:0000369
- 1 of 6 reported patients
- NystagmusHPOHP:0000639
- 1 of 6 reported patients
- Rod-cone dystrophyHPOHP:0000510
- 1 of 6 reported patients
- SeizureHPOHP:0001250
- 1 of 6 reported patients
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.
- TRIP13HGNC:12307
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
- Strong · G2P · Autosomal recessive · 2017
- Moderate · PanelApp Australia · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2020