Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Prader-Willi syndrome
Lissencephaly type 1 due to doublecortin gene mutation
Frequent (30-79%)
Charcot-Marie-Tooth disease type 4A
Very frequent (80-99%)
Congenital muscular dystrophy with intellectual disability
Frequent (30-79%)
Saturnine poisoning
Occasional (5-29%)
Speech-language disorder type 1
Occasional (5-29%)
Related Symptoms
Finding related to ability to moveFinding related to ability to move body partFinding related to ability to control positionFinding related to ability to control postureFinding related to ability to accept base of supportFinding related to ability to perform general purpose physical activitiesWide base of supportNarrow base of supportAble to move items around homeDoes not move items around home
Quick Facts
- SNOMED CT
- 228147004
- UMLS CUI
- C0556280
- Fully Specified Name
- Gross motor impairment (finding)
- Associated Conditions
- 6
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.