Overview
Sporadic foetal brain disruption sequence 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.
Cerebral cortex atrophy
Very frequent (80-99%)HP:0002120
Decreased size of cranium
Very frequent (80-99%)HP:0000252
Dull intelligence
Very frequent (80-99%)HP:0001249
Flattening of cranial vault
Very frequent (80-99%)HP:0001357
Global developmental delay, severe
Very frequent (80-99%)HP:0011344
Involuntary muscle stiffness, contraction, or spasm
Very frequent (80-99%)HP:0001257
Mental retardation, severe
Very frequent (80-99%)HP:0010864
Prominent back of the head
Very frequent (80-99%)HP:0000269
Absent/underdeveloped thymus
Occasional (5-29%)HP:0010515
Adrenal abnormalities
Occasional (5-29%)HP:0000834
Quick Facts
- SNOMED CT
- 763717004
- UMLS CUI
- C4706553
- Fully Specified Name
- Sporadic fetal brain disruption sequence (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.