← Back to Conditions
DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
disorderSNOMED 783619003CUI C5191008
Overview
DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion 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.
Brain imaging abnormality
Very frequent (80-99%)HP:0410263
Feeding difficulties
Very frequent (80-99%)HP:0011968
Funny looking face
Very frequent (80-99%)HP:0001999
Gait disturbance
Very frequent (80-99%)HP:0001288
Mental deficiency
Very frequent (80-99%)HP:0001249
Psychomotor development deficiency
Very frequent (80-99%)HP:0001263
Abnormalities of the toes
Frequent (30-79%)HP:0001780
Ataxia
Frequent (30-79%)HP:0001251
Birth weight less than 10th percentile
Frequent (30-79%)HP:0001518
CNS hypomyelination
Frequent (30-79%)HP:0003429
Convex bridge of nose
Frequent (30-79%)HP:0000426
Decreased body height
Frequent (30-79%)HP:0004322
Decreased size of cranium
Frequent (30-79%)HP:0000252
Difficulty speaking
Frequent (30-79%)HP:0002465
Dilated cerebral ventricle
Frequent (30-79%)HP:0002119
Dyschezia
Frequent (30-79%)HP:0002019
Eye disease
Frequent (30-79%)HP:0000478
Failure to thrive in first year of life
Frequent (30-79%)HP:0001531
Foot deformity
Frequent (30-79%)HP:0001760
Genitourinary dysplasia
Frequent (30-79%)HP:0000119
Hypoplasia of the brainstem
Frequent (30-79%)HP:0002365
Neurohypophysis hypoplasia
Frequent (30-79%)HP:0011757
Nonverbal
Frequent (30-79%)HP:0001344
Seizures
Frequent (30-79%)HP:0001250
Small for gestational age infant
Frequent (30-79%)HP:0001511
Tapering fingers
Frequent (30-79%)HP:0001182
Webbed second, third and fourth toes
Frequent (30-79%)HP:0005768
Wide based walk
Frequent (30-79%)HP:0002136
Abnormality of optic chiasm morphology
Occasional (5-29%)HP:0025163
Anxiety disease
Occasional (5-29%)HP:0000739
Quick Facts
- SNOMED CT
- 783619003
- UMLS CUI
- C5191008
- Fully Specified Name
- Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
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.