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Werner syndrome

disorder
SNOMED 51626007CUI C0043119

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Achilles tendon calcification
Always present (100%)HP:0025441
Alanine aminotransferase increased
Always present (100%)HP:0031964
Baldness
Always present (100%)HP:0002293
Bird-like facial appearance
Always present (100%)HP:0000320
Body ache
Always present (100%)HP:0033047
Decreased bone mineral density Z score
Always present (100%)HP:0004349
Diabetes mellitus
Always present (100%)HP:0000819
Dystrophic nails
Always present (100%)HP:0008404
Elevated glycated haemoglobin
Always present (100%)HP:0040217
Elevated serum aspartate aminotransferase
Always present (100%)HP:0031956
High pitched voice
Always present (100%)HP:0001620
Hyperglycemia
Always present (100%)HP:0003074
Increased triglycerides
Always present (100%)HP:0002155
Low back pain
Always present (100%)HP:0003419
Plantar hyperkeratosis
Always present (100%)HP:0007556
Progeroid facial appearance
Always present (100%)HP:0005328
Skin degeneration
Always present (100%)HP:0004334
Abnormal hair whorl
Very frequent (80-99%)HP:0010721
Abnormality of the chest
Very frequent (80-99%)HP:0000765
Atrophy of fat
Very frequent (80-99%)HP:0100578
Bone cell cancer
Very frequent (80-99%)HP:0002669
Decreased activity of gonads
Very frequent (80-99%)HP:0000135
Decreased body height
Very frequent (80-99%)HP:0004322
Hooked nose
Very frequent (80-99%)HP:0000444
Lens opacities
Very frequent (80-99%)HP:0000518
Osteoporosis
Very frequent (80-99%)HP:0000939
Pili torti
Very frequent (80-99%)HP:0003777
Poliosis of anterior hair
Very frequent (80-99%)HP:0002211
Premature graying of the hair
Very frequent (80-99%)HP:0002216
Premature hardening of arteries
Very frequent (80-99%)HP:0005177

Related Conditions

Multiple malformation syndrome with senile-like appearance(parent)
Disorder of stature(parent)
Congenital anomaly of skin(parent)
Premature ageing syndrome(parent)
Hereditary neoplastic syndrome(parent)
Recessive hereditary disorder (autosomal)(parent)
Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT
51626007
UMLS CUI
C0043119
Fully Specified Name
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.