Overview
Non-distal deletion 10q 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.
Ataxia
Very frequent (80-99%)HP:0001251
Bilateral single transverse palmar creases
Very frequent (80-99%)HP:0007598
Central hypotonia
Very frequent (80-99%)HP:0001252
Cognitive deficits
Very frequent (80-99%)HP:0100543
Gait disturbance
Very frequent (80-99%)HP:0001288
Palpebronasal fold
Very frequent (80-99%)HP:0000286
Squint
Very frequent (80-99%)HP:0000486
Mongoloid slant
Frequent (30-79%)HP:0000582
Brachydactyly
Occasional (5-29%)HP:0001156
Broad flat nasal bridge
Occasional (5-29%)HP:0000431
Curvature of little finger
Occasional (5-29%)HP:0004209
Decreased width of the skull
Occasional (5-29%)HP:0004422
Eye drop
Occasional (5-29%)HP:0000508
Overlapping fingers
Occasional (5-29%)HP:0010557
Unibrow
Occasional (5-29%)HP:0000664
Related Conditions
Quick Facts
- SNOMED CT
- 770665005
- UMLS CUI
- C4749375
- Fully Specified Name
- Non-distal monosomy 10q (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 15
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.