Lissencephaly co-occurrent with congenital cerebellar hypoplasia

disorder

SNOMED 715817007CUI C4274995

Overview

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

Related Conditions

Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B(child)

Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C(child)

Lissencephaly with cerebellar hypoplasia type D(child)

Lissencephaly with cerebellar hypoplasia type F(child)

Lissencephaly with cerebellar hypoplasia type E(child)

Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A(child)

Congenital cerebellar hypoplasia(parent)

Lissencephaly(parent)

Genetic disease(parent)

Quick Facts

SNOMED CT: 715817007
UMLS CUI: C4274995
Fully Specified Name: Lissencephaly co-occurrent with congenital cerebellar hypoplasia (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.