Overview
MYT1L-related Prader-Willi-like syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
ASD
Very frequent (80-99%)HP:0000729
Cognitive delay
Very frequent (80-99%)HP:0001263
Delayed fine motor development
Very frequent (80-99%)HP:0010862
Mental deficiency
Very frequent (80-99%)HP:0001249
Speech and language difficulties
Very frequent (80-99%)HP:0000750
Abnormal eating behaviour
Frequent (30-79%)HP:0100738
Abnormality of coordination
Frequent (30-79%)HP:0011443
Almond shaped eyes
Frequent (30-79%)HP:0007874
Bulbous nose
Frequent (30-79%)HP:0000414
Childhood attention deficit/hyperactivity disorder
Frequent (30-79%)HP:0007018
Cupid-bow shaped upper lip
Frequent (30-79%)HP:0002263
Deep set eye
Frequent (30-79%)HP:0000490
Delayed motor milestones
Frequent (30-79%)HP:0001270
Hypertrophy of cheeks
Frequent (30-79%)HP:0000293
Hypotonia, early
Frequent (30-79%)HP:0008947
Impulsivity
Frequent (30-79%)HP:0100710
Increased appetite
Frequent (30-79%)HP:0002591
Moderate mental retardation
Frequent (30-79%)HP:0002342
Obesity
Frequent (30-79%)HP:0001513
physical aggression
Frequent (30-79%)HP:0000718
Repetitive behaviour Stereotypic behaviour
Frequent (30-79%)HP:0000733
Specific learning disability
Frequent (30-79%)HP:0001328
Tiredness
Frequent (30-79%)HP:0012378
Trouble sleeping
Frequent (30-79%)HP:0002360
Abnormal curving of the cornea or lens of the eye
Occasional (5-29%)HP:0000483
Abnormal temper tantrums
Occasional (5-29%)HP:0025160
Anxiety disease
Occasional (5-29%)HP:0000739
Bruxism
Occasional (5-29%)HP:0003763
Congenital hypotonia
Occasional (5-29%)HP:0001319
Cryptorchidism
Occasional (5-29%)HP:0000028
Quick Facts
- SNOMED CT
- 1303866001
- UMLS CUI
- C5816753
- Fully Specified Name
- Myelin transcription factor 1 like-related developmental delay, intellectual disability, obesity syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.