Microcephaly, polymicrogyria, corpus callosum agenesis syndrome

disorder

SNOMED 773305003CUI C4750772

Overview

Microcephaly, polymicrogyria, corpus callosum agenesis syndrome 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.

Absence of corpus callosum

Frequent (30-79%)HP:0001274

Dilated cerebral ventricle

Frequent (30-79%)HP:0002119

Head circumference small for gestational age

Frequent (30-79%)HP:0011451

Laboured breathing

Frequent (30-79%)HP:0002098

More grooves in brain

Frequent (30-79%)HP:0002126

Small cerebellum

Frequent (30-79%)HP:0001321

Susceptibility to infection

Frequent (30-79%)HP:0002719

Related Conditions

Microgyria(parent)

Recessive hereditary disorder (autosomal)(parent)

Agenesis of corpus callosum(parent)

Hereditary disorder of nervous system(parent)

Multiple system malformation syndrome(parent)

Developmental hereditary disorder(parent)

Congenital microcephalus(parent)

Quick Facts

SNOMED CT: 773305003
UMLS CUI: C4750772
Fully Specified Name: Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 7

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.