Overview
Exencephaly 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.
Abnormal brain morphology
Frequent (30-79%)HP:0012443
Abnormality of cranium
Frequent (30-79%)HP:0002683
Abnormality of the skull bones
Frequent (30-79%)HP:0000929
Absence of corpus callosum
Frequent (30-79%)HP:0001274
Cerebellar hypoplasia/atrophy
Frequent (30-79%)HP:0007360
Hydramnios
Frequent (30-79%)HP:0001561
Prominent eyes
Frequent (30-79%)HP:0000520
Single brain ventricle
Frequent (30-79%)HP:0001360
Thin bone of forehead
Frequent (30-79%)HP:0005466
Anomaly of facial skeleton
Occasional (5-29%)HP:0011821
Anterior pituitary hypoplasia
Occasional (5-29%)HP:0010627
Depressed nasal root/bridge
Occasional (5-29%)HP:0005280
Low-set ears
Occasional (5-29%)HP:0000369
Posterior pituitary agenesis
Occasional (5-29%)HP:0011756
Quick Facts
- SNOMED CT
- 84461004
- UMLS CUI
- C0266453
- Fully Specified Name
- Exencephaly (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 14
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.