Overview
Huriez 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.
Aplasia/Hypoplasia of the skin
Very frequent (80-99%)HP:0008065
Dry skin
Very frequent (80-99%)HP:0000958
Keratoderma
Very frequent (80-99%)HP:0000982
Lack of skin elasticity
Very frequent (80-99%)HP:0100679
Nail disease
Very frequent (80-99%)HP:0001597
Sclerodactyly
Very frequent (80-99%)HP:0011838
Squamous skin carcinoma
Occasional (5-29%)HP:0006739
Adermatoglyphia
HP:0007455
Congenital palmoplantar keratodermia
HP:0007545
Dystrophic nails
HP:0008404
Small nail
HP:0001792
Tapering fingers
HP:0001182
Thickening of upper layer of skin
HP:0025092
Related Conditions
Congenital keratoderma(parent)
Autosomal dominant hereditary disorder(parent)
Hereditary diffuse palmoplantar keratoderma(parent)
Congenital anomaly of skin(parent)
Congenital deformity and malformation of feet and toes(parent)
Congenital abnormality of hand and digits(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 239076000
- UMLS CUI
- C0406767
- Fully Specified Name
- Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 13
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.