Intellectual disability, severe speech delay, mild dysmorphism syndrome

disorder

SNOMED 774203000CUI C4751594

Overview

Intellectual disability, severe speech delay, mild dysmorphism 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.

Communication delay

Very frequent (80-99%)HP:0002474

Delayed language development

Very frequent (80-99%)HP:0000750

Protruding forehead

Very frequent (80-99%)HP:0011220

Speech articulation difficulties

Very frequent (80-99%)HP:0009088

Abnormality of refraction

Frequent (30-79%)HP:0000539

Anxiety disease

Frequent (30-79%)HP:0000739

Autism spectrum disorder

Frequent (30-79%)HP:0000729

Behavioral symptoms

Frequent (30-79%)HP:0000708

Brain imaging abnormality

Frequent (30-79%)HP:0410263

Broad, upturned nose

Frequent (30-79%)HP:0000455

Cardiac anomaly

Frequent (30-79%)HP:0001627

Deep nasolabial crease

Frequent (30-79%)HP:0005272

Delayed motor milestones

Frequent (30-79%)HP:0001270

Down-slanting palpebral fissure

Frequent (30-79%)HP:0000494

Downturned corners of mouth

Frequent (30-79%)HP:0002714

Dyschezia

Frequent (30-79%)HP:0002019

Eye disease

Frequent (30-79%)HP:0000478

Eyelid ptosis

Frequent (30-79%)HP:0000508

Feeding difficulties

Frequent (30-79%)HP:0011968

Flexion contractures

Frequent (30-79%)HP:0001371

Frontal upsweep of hair

Frequent (30-79%)HP:0002236

Horizontal chin skin cleft

Frequent (30-79%)HP:0011823

Increased distance between eyes

Frequent (30-79%)HP:0000316

Increased size of mandible

Frequent (30-79%)HP:0000303

Involuntary muscle stiffness, contraction, or spasm

Frequent (30-79%)HP:0001257

Mental retardation, severe

Frequent (30-79%)HP:0010864

Moderate mental retardation

Frequent (30-79%)HP:0002342

Oromotor apraxia

Frequent (30-79%)HP:0007301

Poor attention span

Frequent (30-79%)HP:0000736

Poor weight gain

Frequent (30-79%)HP:0001508

Related Conditions

Multiple malformation syndrome with facial defects as major feature(parent)

Global developmental delay(parent)

Genetic intellectual disability(parent)

Quick Facts

SNOMED CT: 774203000
UMLS CUI: C4751594
Fully Specified Name: Intellectual disability, severe speech delay, mild dysmorphism 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.