Prader-Willi syndrome due to translocation
MONDO:0015785Mondo
Findings
No curated finding names Prader-Willi syndrome due to translocation yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
93 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.
- Feeding difficulties in infancyHPOHP:0008872
- Very frequent (80% to 99% of cases)
- ObesityHPOHP:0001513
- Very frequent (80% to 99% of cases)
- Poor suckHPOHP:0002033
- Very frequent (80% to 99% of cases)
- Weak cryHPOHP:0001612
- Very frequent (80% to 99% of cases)
- Abnormal facial shapeHPOHP:0001999
- Frequent (30% to 79% of cases)
- Abnormal temper tantrumsHPOHP:0025160
- Frequent (30% to 79% of cases)
- Almond-shaped palpebral fissureHPOHP:0007874
- Frequent (30% to 79% of cases)
- Anterior pituitary hypoplasiaHPOHP:0010627
- Frequent (30% to 79% of cases)
- Decreased response to growth hormone stimulation testHPOHP:0000824
- Frequent (30% to 79% of cases)
- Downturned corners of mouthHPOHP:0002714
- Frequent (30% to 79% of cases)
- External genital hypoplasiaHPOHP:0003241
- Frequent (30% to 79% of cases)
- Hypogonadotropic hypogonadismHPOHP:0000044
- Frequent (30% to 79% of cases)
Show the remaining 81
- Mild intellectual disabilityHPOHP:0001256
- Frequent (30% to 79% of cases)
- Narrow foreheadHPOHP:0000341
- Frequent (30% to 79% of cases)
- Neonatal hypotoniaHPOHP:0001319
- Frequent (30% to 79% of cases)
- Recurrent respiratory infectionsHPOHP:0002205
- Frequent (30% to 79% of cases)
- Respiratory distressHPOHP:0002098
- Frequent (30% to 79% of cases)
- Severe muscular hypotoniaHPOHP:0006829
- Frequent (30% to 79% of cases)
Where it sits
- A kind of