Overview
Speech-language disorder type 1 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.
Abnormal vocalization
Very frequent (80-99%)HP:0002167
Delayed language development
Very frequent (80-99%)HP:0000750
Abnormal prosody
Frequent (30-79%)HP:0031434
Communication delay
Frequent (30-79%)HP:0002474
Deficit in grammar
Frequent (30-79%)HP:0006977
Difficulty articulating speech
Frequent (30-79%)HP:0001260
Fine motor skill dysfunction
Frequent (30-79%)HP:0007010
Incomprehensible speech
Frequent (30-79%)HP:0002546
Problems speaking
Frequent (30-79%)HP:0002465
Receptive language delay
Frequent (30-79%)HP:0010863
Specific learning disability
Frequent (30-79%)HP:0001328
Speech dyspraxia
Frequent (30-79%)HP:0011098
Abnormal caudate nucleus morphology
Occasional (5-29%)HP:0002339
Caudate degeneration
Occasional (5-29%)HP:0002340
Delayed milestone development
Occasional (5-29%)HP:0012434
Drooling
Occasional (5-29%)HP:0002307
Feeding difficulties
Occasional (5-29%)HP:0011968
Poor gross motor coordination
Occasional (5-29%)HP:0007015
ASD
Very rare (1-4%)HP:0000729
Lack of eyebrow curvature
Very rare (1-4%)HP:0011228
Narrow, high-arched roof of mouth
Very rare (1-4%)HP:0002705
Overfolded helix
Very rare (1-4%)HP:0000396
Submucous cleft hard palate
Very rare (1-4%)HP:0000176
Abnormality of the basal ganglia
HP:0002134
Oromotor apraxia
HP:0007301
Quick Facts
- SNOMED CT
- 1365977003
- UMLS CUI
- C0750927
- Fully Specified Name
- Isolated childhood apraxia of speech (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 25
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.