Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome

disorder

SNOMED 720813007CUI C4304196

Overview

Craniosynostosis with Dandy-Walker malformation and hydrocephalus 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.

Dandy-Walker cyst

Very frequent (80-99%)HP:0001305

Frontal protuberance

Very frequent (80-99%)HP:0002007

Hypoplastic mandible

Very frequent (80-99%)HP:0000347

Increased distance between eyes

Very frequent (80-99%)HP:0000316

Narrow cranium shape

Very frequent (80-99%)HP:0000268

Nonsyndromal hydrocephalus

Very frequent (80-99%)HP:0000238

Optic atrophy

Very frequent (80-99%)HP:0000648

Orbital craniosynostosis

Very frequent (80-99%)HP:0005472

Small cerebellum

Very frequent (80-99%)HP:0001321

Low intelligence

Frequent (30-79%)HP:0001249

Squint

Frequent (30-79%)HP:0000486

Related Conditions

Autosomal dominant hereditary disorder(parent)

Dandy-Walker syndrome(parent)

Craniosynostosis syndrome(parent)

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

Hereditary disorder of musculoskeletal system(parent)

Hereditary disorder of nervous system(parent)

Disorder of skull(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 720813007
UMLS CUI: C4304196
Fully Specified Name: Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 11

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.