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Fetal microcephaly

disorder
SNOMED 431265009CUI C2315667

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Sporadic foetal brain disruption sequence(child)
Lethal fetal cerebrorenogenitourinary agenesis or hypoplasia syndrome(child)
COASY gene related pontocerebellar hypoplasia(child)
Disorder of head(parent)
Fetal growth abnormality(parent)

Quick Facts

SNOMED CT
431265009
UMLS CUI
C2315667
Fully Specified Name
Fetal microcephaly (disorder)
Specialists
0
Diagnostic Biomarkers
0
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.