Premature ageing appearance, developmental delay, cardiac arrhythmia syndrome

disorder

SNOMED 771442003CUI C3275447

Overview

Premature ageing appearance, developmental delay, cardiac arrhythmia 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.

Microvesicular steatosis

Always present (100%)HP:0001414

Apnea

Frequent (30-79%)HP:0002104

Broad big toe

Frequent (30-79%)HP:0010055

Central hypotonia

Frequent (30-79%)HP:0001252

Cognitive delay

Frequent (30-79%)HP:0001263

Eczema

Frequent (30-79%)HP:0000964

Excessive daytime somnolence

Frequent (30-79%)HP:0001262

Feeding difficulties

Frequent (30-79%)HP:0011968

Flared nostrils

Frequent (30-79%)HP:0000454

Generalised decreased muscle tone

Frequent (30-79%)HP:0001290

Hypotrophic eyebrow

Frequent (30-79%)HP:0100840

Increased distance between eyes

Frequent (30-79%)HP:0000316

Increased heart size

Frequent (30-79%)HP:0001640

Minimal subcutaneous fat

Frequent (30-79%)HP:0003717

Narrow palate

Frequent (30-79%)HP:0000189

Scoliosis

Frequent (30-79%)HP:0002650

Short neck

Frequent (30-79%)HP:0000470

Supratentorial atrophy

Frequent (30-79%)HP:0002059

Torticollis

Frequent (30-79%)HP:0000473

Wider-than-typical soft spot of skull

Frequent (30-79%)HP:0000260

Abnormal forehead morphology

Occasional (5-29%)HP:0000290

Abnormal head movements

Occasional (5-29%)HP:0002457

ASD

Occasional (5-29%)HP:0000729

Aspiration

Occasional (5-29%)HP:0002835

Atrial premature complex

Occasional (5-29%)HP:0006699

Behavioural/Psychiatric abnormality

Occasional (5-29%)HP:0000708

Bicuspid aortic valve

Occasional (5-29%)HP:0001647

Bilateral ptosis

Occasional (5-29%)HP:0001488

Capillary malformation

Occasional (5-29%)HP:0025104

Cardiogenic shock

Occasional (5-29%)HP:0030149

Related Conditions

X-linked hereditary disease(parent)

Premature ageing syndrome(parent)

Fetal and/or neonatal disorder of integument(parent)

Quick Facts

SNOMED CT: 771442003
UMLS CUI: C3275447
Fully Specified Name: Ogden 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.