Overview
Finnish upper limb onset distal myopathy 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.
Amyotrophy of ankle musculature
Frequent (30-79%)HP:0009031
Clumsiness
Frequent (30-79%)HP:0002312
Contractures of the hands
Frequent (30-79%)HP:0009473
EMG: myopathic changes
Frequent (30-79%)HP:0003458
Fatty replacement of skeletal muscle
Frequent (30-79%)HP:0012548
Gait disturbance
Frequent (30-79%)HP:0001288
Intrinsic hand muscle atrophy
Frequent (30-79%)HP:0008954
Loss of distal sensation
Frequent (30-79%)HP:0002936
Mildly elevated creatine kinase
Frequent (30-79%)HP:0008180
Muscle weakness, progressive, distal
Frequent (30-79%)HP:0009063
Rimmed vacuoles
Frequent (30-79%)HP:0003805
Steppage gait
Frequent (30-79%)HP:0003376
Weakness of the intrinsic hand muscles
Frequent (30-79%)HP:0009005
Muscle weakness, progressive, proximal
Occasional (5-29%)HP:0009073
Split hand
Occasional (5-29%)HP:0001171
Distal muscle atrophy, upper and lower limbs
HP:0003693
Foot deformity
HP:0001760
Late-onset proximal muscle weakness
HP:0003694
Muscular dystrophy
HP:0003560
Weakness of outermost muscles
HP:0002460
Quick Facts
- SNOMED CT
- 763718009
- UMLS CUI
- C1864706
- Fully Specified Name
- Finnish upper limb onset distal myopathy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
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.