MYT1L-related Prader-Willi-like syndrome

disorder

SNOMED 1303866001CUI C5816753

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

Delayed fine motor development

Very frequent (80-99%)HP:0010862

Delayed language development

Very frequent (80-99%)HP:0000750

Mental and motor retardation

Very frequent (80-99%)HP:0001263

Mental-retardation

Very frequent (80-99%)HP:0001249

Abnormal eating behaviour

Frequent (30-79%)HP:0100738

Abnormality of coordination

Frequent (30-79%)HP:0011443

Aggression

Frequent (30-79%)HP:0000718

Almond shaped eyes

Frequent (30-79%)HP:0007874

Childhood attention deficit/hyperactivity disorder

Frequent (30-79%)HP:0007018

Cupid-bow shaped upper lip

Frequent (30-79%)HP:0002263

Delayed motor milestones

Frequent (30-79%)HP:0001270

Enophthalmos

Frequent (30-79%)HP:0000490

Hyperphagia

Frequent (30-79%)HP:0002591

Hypertrophy of cheeks

Frequent (30-79%)HP:0000293

Hypotonia, early

Frequent (30-79%)HP:0008947

Impulsivity

Frequent (30-79%)HP:0100710

Moderate mental retardation

Frequent (30-79%)HP:0002342

Obesity

Frequent (30-79%)HP:0001513

Potato nose

Frequent (30-79%)HP:0000414

Specific learning disability

Frequent (30-79%)HP:0001328

Stimming

Frequent (30-79%)HP:0000733

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

Related Conditions

Developmental delay(parent)

Genetic obesity disorder(parent)

Genetic intellectual disability(parent)

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.