Axial muscle weakness

Symptom Information:

Symptom ID: HPO:0003327
Synonyms:
Axial muscle weakness [OMIM:Axial muscle weakness]
Quality:
Cross references:
OMIM: "Axial muscle weakness" [OMIM:Axial muscle weakness]
Is a (Direct Parents):
HPO         Muscle weakness
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Muscle weakness(HPO:0001324)
                Axial muscle weakness(HPO:0003327)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Antenatal multiminicore disease with arthrogryposis multiplex congenita (Orphanet:178148)
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures (Orphanet:363454)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive limb girdle muscular dystrophy type 2A (Orphanet:267)
Autosomal recessive limb-girdle muscular dystrophy type 2E (Orphanet:119)
Classic multiminicore myopathy (Orphanet:324604)
Congenital multicore myopathy with external ophthalmoplegia (Orphanet:98905)
Desmin-related myopathy with Mallory body-like inclusions (Orphanet:84132)
MYOPATHY, CENTRONUCLEAR, 5 (OMIM:615959)
Rigid spine syndrome (Orphanet:97244)