Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Cerebellar vermis aplasia
HP:0002335
Cranial nerve paralysis
HP:0006824
Dilated fourth ventricle
HP:0002198
Instability or lack of coordination of central trunk muscles
HP:0002078
Involuntary, rapid, rhythmic eye movements
HP:0000639
Nonsyndromal hydrocephalus
HP:0000238
Partial absence of cerebellar vermis
HP:0002951
Posterior fossa cyst at the fourth ventricle
HP:0000933
Thinning and bulging of posterior skull bones
HP:0000931
Thinning and bulging of posterior skull bones over the transverse sinuses
HP:0000930
Related Conditions
Dandy-Walker syndrome with spina bifida(child)
Hydrocephalus with cleft palate and joint contracture syndrome(child)
X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome(child)
Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome(child)
Macrocephaly, short stature, paraplegia syndrome(child)
Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome(child)
Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome(child)
Dandy-Walker malformation with postaxial polydactyly syndrome(child)
Congenital hydrocephalus(parent)
Cystic malformation of posterior fossa(parent)
Congenital cerebellar hypoplasia(parent)
Quick Facts
- SNOMED CT
- 14447001
- UMLS CUI
- C0010964
- Fully Specified Name
- Dandy-Walker syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 10
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.