Lissencephaly type 3 familial fetal akinesia sequence syndrome

disorder

SNOMED 718719001CUI C4305255

Overview

Lissencephaly type 3 familial fetal akinesia sequence syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Hereditary disorder of nervous system(parent)

Developmental hereditary disorder(parent)

Microlissencephaly(parent)

Quick Facts

SNOMED CT: 718719001
UMLS CUI: C4305255
Fully Specified Name: Lissencephaly type 3 familial fetal akinesia sequence syndrome (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.