autosomal dominant distal myopathy
MONDO:0016108Mondo
Findings
No curated finding names autosomal dominant distal myopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Autosomal dominant form of distal myopathy.
Definition from the Mondo Disease Ontology (MONDO:0016108), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (15)
- adult-onset distal myopathy due to VCP mutation
- asymetric thumb-handgrip weakness-distal myopathy
- calf-predominant weakness-gastrocnemius medialis atrophy-distal myopathy
- distal myopathy with posterior leg and anterior hand involvement
- distal myopathy with vocal cord weakness
- distal myopathy, Tateyama type
- distal myopathy, Welander type
- Finnish upper limb-onset distal myopathy
- KLHL9-related early-onset distal myopathy
- myofibrillar myopathy 2
- myofibrillar myopathy 3
- myofibrillar myopathy 4
- myopathy, myofibrillar, 9, with early respiratory failure
- TARDBP-related predominantly upper-limb distal myopathy
- tibial muscular dystrophy
Other names
1 name
Resolves to: autosomal dominant distal myopathy
- Also called
- distal myopathy, autosomal dominant