Finnish upper limb-onset distal myopathy
Findings
No curated finding names Finnish upper limb-onset distal myopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Finnish upper limb-onset distal myopathy is a rare, genetic distal myopathy characterized by slowly progressive distal to proximal limb muscle weakness and atrophy, with characteristic early involvement of thenar and hypothenar muscles. Patients present with clumsiness of the hands and stumbling in the fourth to fifth decade of life, and later develop steppage gait and contractures of the hands. Progressive fatty degeneration affects intrinsic muscles of the hands, gluteus medium and both anterior and posterior compartment muscles of the distal lower extremities, with later involvement of forearm muscles, triceps, infraspinatus and the proximal lower limb muscles. Asymmetry of muscle involvement is common.
Definition from the Mondo Disease Ontology (MONDO:0012410), read 2026-09-29. CC BY 4.0.
Features
15 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Amyotrophy of ankle musculatureHPOHP:0009031
- Frequent (30% to 79% of cases)
- ClumsinessHPOHP:0002312
- Frequent (30% to 79% of cases)
- Distal sensory impairmentHPOHP:0002936
- Frequent (30% to 79% of cases)
- EMG: myopathic abnormalitiesHPOHP:0003458
- Frequent (30% to 79% of cases)
- Fatty replacement of skeletal muscleHPOHP:0012548
- Frequent (30% to 79% of cases)
- Gait disturbanceHPOHP:0001288
- Frequent (30% to 79% of cases)
- Intrinsic hand muscle atrophy
Show the remaining 3
- Weakness of the intrinsic hand musclesHPOHP:0009005
- Frequent (30% to 79% of cases)
- Progressive proximal muscle weaknessHPOHP:0009073
- Occasional (5% to 29% of cases)
- Split handHPOHP:0001171
- Occasional (5% to 29% of cases)
Where it sits
- A kind of
Other names
2 names
Resolves to: Finnish upper limb-onset distal myopathy
- Also called
- distal myopathy type 3MPD3