DVD - Developmental verbal apraxia

disorder

SNOMED 229703009CUI C5441570

Overview

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

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormality of the basal ganglia

HP:0002134

Deficit in grammar

HP:0006977

Incomprehensible speech

HP:0002546

Oromotor apraxia

HP:0007301

Speech delay

HP:0000750

Related Conditions

Speech-language disorder type 1(child)

Apraxia of phonation(parent)

Verbal dyspraxia(parent)

Quick Facts

SNOMED CT: 229703009
UMLS CUI: C5441570
Fully Specified Name: Childhood apraxia of speech (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.