Weaver Williams syndrome

disorder

SNOMED 726670008CUI C0796198

Overview

Weaver Williams 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.

Cleft of palate

Always present (100%)HP:0000175

Decreased size of cranium

Always present (100%)HP:0000252

Moderate mental retardation

Always present (100%)HP:0002342

Narrow mouth

Always present (100%)HP:0000160

Protruding ear

Always present (100%)HP:0000411

Weight less than 3rd percentile

Always present (100%)HP:0004325

Mental retardation, severe

Occasional (5-29%)HP:0010864

Related Conditions

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

Recessive hereditary disorder (autosomal)(parent)

Cleft palate(parent)

Developmental hereditary disorder(parent)

Genetic intellectual disability(parent)

Quick Facts

SNOMED CT: 726670008
UMLS CUI: C0796198
Fully Specified Name: Weaver Williams syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 7

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.