Fetal valproate syndrome

disorder

SNOMED 17231009CUI C0236026

Overview

Fetal valproate 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.

Decreased volume of lip vermillion

Very frequent (80-99%)HP:0000233

Downturned corners of mouth

Very frequent (80-99%)HP:0002714

Increased length of philtrum

Very frequent (80-99%)HP:0000343

Narrow mouth

Very frequent (80-99%)HP:0000160

Nasal hypoplasia

Very frequent (80-99%)HP:0003196

Omphalocoele

Very frequent (80-99%)HP:0001539

Palpebronasal fold

Very frequent (80-99%)HP:0000286

Retruded nasal dorsum

Very frequent (80-99%)HP:0000457

Related Conditions

Fetal disorder caused by anticonvulsant via placental transfer(parent)

Disorder of foetal structure(parent)

Disorder caused by psychoactive substance(parent)

Foetal disorder caused by chemicals(parent)

Quick Facts

SNOMED CT: 17231009
UMLS CUI: C0236026
Fully Specified Name: Fetal valproate syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

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.