SIM1-related Prader-Willi-like syndrome
MONDO:0018355Mondo
Findings
No curated finding names SIM1-related Prader-Willi-like syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
63 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.
- Abnormal facial shapeHPOHP:0001999
- Very frequent (80% to 99% of cases)
- CryptorchidismHPOHP:0000028
- Very frequent (80% to 99% of cases)
- Floppy infantHPOHP:0008947
- Very frequent (80% to 99% of cases)
- HypogonadismHPOHP:0000135
- Very frequent (80% to 99% of cases)
- InfertilityHPOHP:0000789
- Very frequent (80% to 99% of cases)
- Motor delayHPOHP:0001270
- Very frequent (80% to 99% of cases)
- ObesityHPOHP:0001513
- Very frequent (80% to 99% of cases)
- Abdominal obesityHPOHP:0012743
- Frequent (30% to 79% of cases)
- Abnormal temper tantrumsHPOHP:0025160
- Frequent (30% to 79% of cases)
- Absence of pubertal developmentHPOHP:0008197
- Frequent (30% to 79% of cases)
- Atypical behaviorHPOHP:0000708
- Frequent (30% to 79% of cases)
- Autistic behaviorHPOHP:0000729
- Frequent (30% to 79% of cases)
Show the remaining 51
- Brain imaging abnormalityHPOHP:0410263
- Frequent (30% to 79% of cases)
- Clitoral hypoplasiaHPOHP:0000060
- Frequent (30% to 79% of cases)
- Decreased testicular sizeHPOHP:0008734
- Frequent (30% to 79% of cases)
- Delayed speech and language developmentHPOHP:0000750
- Frequent (30% to 79% of cases)
- Diminished deep tendon reflexHPOHP:0001315
- Frequent (30% to 79% of cases)
- External genital hypoplasiaHPOHP:0003241
- Frequent (30% to 79% of cases)
Where it sits
- A kind of
Other names
1 name
Resolves to: SIM1-related Prader-Willi-like syndrome
- Also called
- SIM1-related PWLS