Overview
Scleromyxoedema is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Research Evidence
Peer-reviewed studies linked via MeSH term "Scleromyxedema" from the MEDLINE/PubMed database.
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Scleromyxedema treatment: a systematic review and update.
[object Object], [object Object], [object Object] · Int J Dermatol · 2020
PMID: 32358980Meta-Analysis
Hyalase in Dermatology: Applications Beyond Filler Management.
[object Object], [object Object], [object Object] et al. · J Cosmet Dermatol · 2025
Sclerosing diseases of the skin.
[object Object], [object Object], [object Object] et al. · J Dtsch Dermatol Ges · 2025
Nodular-Type Lichen Myxedematosus: A Rare Variant With Exclusive Involvement of the Hands-Report of Two Cases With a Comprehensive Review of the Literature.
[object Object], [object Object] · Am J Dermatopathol · 2024
PMID: 37982501Review
Consensus statement on the diagnosis and treatment of sclerosing diseases of the skin, Part 2: Scleromyxoedema and scleroedema.
[object Object], [object Object], [object Object] et al. · J Eur Acad Dermatol Venereol · 2024
PMID: 38456518Review
[Scleromyxedema].
[object Object], [object Object], [object Object] · Dermatologie (Heidelb) · 2024
PMID: 38363313Review
New and emerging conditions of acquired cutaneous mucinoses in adults.
[object Object] · J Eur Acad Dermatol Venereol · 2022
PMID: 35124832Review
[Mimetics of systemic sclerosis].
[object Object], [object Object], [object Object] · Z Rheumatol · 2019
PMID: 30255410Review
Lichen myxedematosus: a rare group of cutaneous mucinosis.
[object Object], [object Object], [object Object] · An Bras Dermatol · 2019
Search all PubMed articles for Scleromyxoedema
Research data from MEDLINE/PubMed
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Generalized abnormality of skin
Very frequent (80-99%)HP:0011354
Papules
Very frequent (80-99%)HP:0200034
Paraproteinemia
Very frequent (80-99%)HP:0031047
Abnormal forearm morphology
Frequent (30-79%)HP:0002973
Abnormal hands
Frequent (30-79%)HP:0001155
Arthralgias
Frequent (30-79%)HP:0002829
Deglutition disorder
Frequent (30-79%)HP:0002015
Diffusely thickened skin
Frequent (30-79%)HP:0001072
Disorder of face
Frequent (30-79%)HP:0000271
Elevated circulating creatine phosphokinase
Frequent (30-79%)HP:0003236
Glabellar abnormality
Frequent (30-79%)HP:0002056
Indurated skin
Frequent (30-79%)HP:0030053
Malformation of the neck
Frequent (30-79%)HP:0000464
Myopathy
Frequent (30-79%)HP:0003198
Proximal limb muscle weakness
Frequent (30-79%)HP:0003701
Sclerodactyly
Frequent (30-79%)HP:0011838
Skin-colored papule
Frequent (30-79%)HP:0025512
Abnormality of central nervous system electrophysiology
Occasional (5-29%)HP:0030178
Abnormality of muscle morphology
Occasional (5-29%)HP:0011805
Abnormality of the lungs
Occasional (5-29%)HP:0002088
Aged leonine appearance
Occasional (5-29%)HP:0008509
Cardiovascular disease
Occasional (5-29%)HP:0001626
Encephalopathy
Occasional (5-29%)HP:0001298
Epilepsy
Occasional (5-29%)HP:0001250
Exertional dyspnea
Occasional (5-29%)HP:0002875
Gastroesophageal reflux disease
Occasional (5-29%)HP:0002020
Gastrointestinal disease
Occasional (5-29%)HP:0011024
Intestinal hypoperistalsis
Occasional (5-29%)HP:0100771
Muscle pain
Occasional (5-29%)HP:0003326
Narrow mouth
Occasional (5-29%)HP:0000160
Related Conditions
Quick Facts
- SNOMED CT
- 402468007
- UMLS CUI
- C0263390
- Fully Specified Name
- Scleromyxedema (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.