Overview
Atypical Werner 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.
Abnormal hair morphology
Very frequent (80-99%)HP:0001595
Abnormal hair quantity
Very frequent (80-99%)HP:0011362
Abnormal hair whorl
Very frequent (80-99%)HP:0010721
Abnormality of circulating leptin level
Very frequent (80-99%)HP:0004361
Abnormality of lung artery
Very frequent (80-99%)HP:0004414
Abnormality of the calcaneal tendon
Very frequent (80-99%)HP:0005109
Abnormality of the cerebral blood vessels
Very frequent (80-99%)HP:0100659
Abnormality of the chest
Very frequent (80-99%)HP:0000765
Anomaly of the testes
Very frequent (80-99%)HP:0000035
Aortic valve calcification
Very frequent (80-99%)HP:0004380
Aplasia/Hypoplasia of the skin
Very frequent (80-99%)HP:0008065
Atrophy of fat
Very frequent (80-99%)HP:0100578
Bone cell cancer
Very frequent (80-99%)HP:0002669
Calcium deposits in joints
Very frequent (80-99%)HP:0000934
Cardiac insufficiency
Very frequent (80-99%)HP:0001635
Decreased activity of gonads
Very frequent (80-99%)HP:0000135
Decreased body height
Very frequent (80-99%)HP:0004322
Decreased bone mineral density Z score
Very frequent (80-99%)HP:0004349
Decreased fertility
Very frequent (80-99%)HP:0000144
Decreased volume of lip vermillion
Very frequent (80-99%)HP:0000233
Delayed puberty
Very frequent (80-99%)HP:0000823
Diabetes mellitus
Very frequent (80-99%)HP:0000819
Epidermal hyperkeratosis
Very frequent (80-99%)HP:0000962
Fallen arches
Very frequent (80-99%)HP:0001763
Fasting hyperinsulinemia
Very frequent (80-99%)HP:0008283
Fatty liver
Very frequent (80-99%)HP:0001397
Fragile nails
Very frequent (80-99%)HP:0001808
Generalised sclerosis of hand bones
Very frequent (80-99%)HP:0004054
Glucose in urine
Very frequent (80-99%)HP:0003076
Hair loss
Very frequent (80-99%)HP:0001596
Related Conditions
Quick Facts
- SNOMED CT
- 715633008
- UMLS CUI
- C4275075
- Fully Specified Name
- Atypical Werner syndrome (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.