silver-Russell syndrome due to 11p15 microduplication
MONDO:0016481Mondo
Findings
No curated finding names silver-Russell syndrome due to 11p15 microduplication yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
19 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.
- Clinodactyly of the 5th fingerHPOHP:0004209
- Frequent (30% to 79% of cases)
- Delayed skeletal maturationHPOHP:0002750
- Frequent (30% to 79% of cases)
- Failure to thriveHPOHP:0001508
- Frequent (30% to 79% of cases)
- Intrauterine growth retardationHPOHP:0001511
- Frequent (30% to 79% of cases)
- OligohydramniosHPOHP:0001562
- Frequent (30% to 79% of cases)
- Postnatal growth retardationHPOHP:0008897
- Frequent (30% to 79% of cases)
- Short statureHPOHP:0004322
- Frequent (30% to 79% of cases)
- Small for gestational ageHPOHP:0001518
- Frequent (30% to 79% of cases)
- Triangular faceHPOHP:0000325
- Frequent (30% to 79% of cases)
- Decreased fetal movementHPOHP:0001558
- Occasional (5% to 29% of cases)
- Facial asymmetryHPOHP:0000324
- Occasional (5% to 29% of cases)
- Floppy infantHPOHP:0008947
- Occasional (5% to 29% of cases)
Show the remaining 7
- Midface retrusionHPOHP:0011800
- Occasional (5% to 29% of cases)
- Motor delayHPOHP:0001270
- Occasional (5% to 29% of cases)
- Prominent foreheadHPOHP:0011220
- Occasional (5% to 29% of cases)
- Relative macrocephalyHPOHP:0004482
- Occasional (5% to 29% of cases)
- Severe intrauterine growth retardationHPOHP:0008846
- Occasional (5% to 29% of cases)
- Specific learning disabilityHPOHP:0001328
- Occasional (5% to 29% of cases)