Overview
Lelis syndrome 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.
Acanthosis nigricans
Always present (100%)HP:0000956
Hypohidrosis
Always present (100%)HP:0000966
Thin, sparse hair
Always present (100%)HP:0008070
Abnormal mouth
Very frequent (80-99%)HP:0000153
Dystrophic nails
Frequent (30-79%)HP:0008404
Increased pigmentation around the mouth
Frequent (30-79%)HP:0010802
Lingua plicata
Frequent (30-79%)HP:0000221
Missing between one and six teeth
Frequent (30-79%)HP:0000668
Palmoplantar keratosis
Frequent (30-79%)HP:0000972
Poor school performance
Frequent (30-79%)HP:0001249
Abnormal toenail morphology
Occasional (5-29%)HP:0008388
Absent lower eyelashes
Occasional (5-29%)HP:0007646
Blotchy loss of skin colour
Occasional (5-29%)HP:0001045
Dental cavities
Occasional (5-29%)HP:0000670
High pitched voice
Occasional (5-29%)HP:0001620
Hypotrophic midface
Occasional (5-29%)HP:0011800
Increased size of mandible
Occasional (5-29%)HP:0000303
Laterally sparse eyebrows
Occasional (5-29%)HP:0005338
Mongoloid slant
Occasional (5-29%)HP:0000582
Outward facing eye ball
Occasional (5-29%)HP:0000577
Vertical enlargement of face
Occasional (5-29%)HP:0000276
Yellow nails
Occasional (5-29%)HP:0011367
Quick Facts
- SNOMED CT
- 719429003
- UMLS CUI
- C1842307
- Fully Specified Name
- Ectodermal dysplasia with acanthosis nigricans syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 22
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.