MYT1L-related developmental delay-intellectual disability-obesity syndrome
MONDO:0957477Mondo
Findings
No curated finding names MYT1L-related developmental delay-intellectual disability-obesity syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
64 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.
- Autistic behaviorHPOHP:0000729
- Very frequent (80% to 99% of cases)
- Delayed fine motor developmentHPOHP:0010862
- Very frequent (80% to 99% of cases)
- Delayed speech and language developmentHPOHP:0000750
- Very frequent (80% to 99% of cases)
- Global developmental delayHPOHP:0001263
- Very frequent (80% to 99% of cases)
- Intellectual disabilityHPOHP:0001249
- Very frequent (80% to 99% of cases)
- Abnormal eating behaviorHPOHP:0100738
- Frequent (30% to 79% of cases)
- Abnormality of coordinationHPOHP:0011443
- Frequent (30% to 79% of cases)
- Aggressive behaviorHPOHP:0000718
- Frequent (30% to 79% of cases)
- Almond-shaped palpebral fissureHPOHP:0007874
- Frequent (30% to 79% of cases)
- Attention deficit hyperactivity disorderHPOHP:0007018
- Frequent (30% to 79% of cases)
- Bulbous noseHPOHP:0000414
- Frequent (30% to 79% of cases)
- Deeply set eyeHPOHP:0000490
- Frequent (30% to 79% of cases)
Show the remaining 52
- Exaggerated cupid's bowHPOHP:0002263
- Frequent (30% to 79% of cases)
- FatigueHPOHP:0012378
- Frequent (30% to 79% of cases)
- Floppy infantHPOHP:0008947
- Frequent (30% to 79% of cases)
- Full cheeksHPOHP:0000293
- Frequent (30% to 79% of cases)
- ImpulsivityHPOHP:0100710
- Frequent (30% to 79% of cases)
- Moderate intellectual disabilityHPOHP:0002342
- Frequent (30% to 79% of cases)
Where it sits
- A kind of