silver-Russell syndrome due to an imprinting defect of 11p15
MONDO:0016480Mondo
Findings
No curated finding names silver-Russell syndrome due to an imprinting defect of 11p15 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
28 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.
- Asymmetric growthHPOHP:0100555
- Very frequent (80% to 99% of cases)
- Delayed skeletal maturationHPOHP:0002750
- Very frequent (80% to 99% of cases)
- Short chinHPOHP:0000331
- Very frequent (80% to 99% of cases)
- Short statureHPOHP:0004322
- Very frequent (80% to 99% of cases)
- Small for gestational ageHPOHP:0001518
- Very frequent (80% to 99% of cases)
- Triangular faceHPOHP:0000325
- Very frequent (80% to 99% of cases)
- Clinodactyly of the 5th fingerHPOHP:0004209
- Frequent (30% to 79% of cases)
- Decreased body weightHPOHP:0004325
- Frequent (30% to 79% of cases)
- Dental crowdingHPOHP:0000678
- Frequent (30% to 79% of cases)
- Feeding difficulties in infancyHPOHP:0008872
- Frequent (30% to 79% of cases)
- High palateHPOHP:0000218
- Frequent (30% to 79% of cases)
- Lower limb asymmetryHPOHP:0100559
- Frequent (30% to 79% of cases)
Show the remaining 16
- Postnatal growth retardationHPOHP:0008897
- Frequent (30% to 79% of cases)
- Prominent foreheadHPOHP:0011220
- Frequent (30% to 79% of cases)
- Protruding earHPOHP:0000411
- Frequent (30% to 79% of cases)
- Relative macrocephalyHPOHP:0004482
- Frequent (30% to 79% of cases)
- Upper limb asymmetryHPOHP:0100560
- Frequent (30% to 79% of cases)
- Abnormal external genitalia morphologyHPOHP:0000811
- Occasional (5% to 29% of cases)
Where it sits
- A kind of
Other names
1 name
Resolves to: silver-Russell syndrome due to an imprinting defect of 11p15
- Also called
- Silver-Russell syndrome due to an imprinting defect of type 11p15