Proximal muscle weakness in lower limbs

Symptom Information:

Symptom ID: HPO:0008994
Synonyms:
Muscle weakness, proximal, lower limbs [HPO:0008994]
Muscle weakness, proximal, lower limbs [OMIM:Muscle weakness, proximal, lower limbs]
Proximal muscle weakness in lower limbs [OMIM:Proximal muscle weakness in lower limbs]
Lower limb muscle weakness, proximal [OMIM:Lower limb muscle weakness, proximal]
Quality:
Cross references:
OMIM: "Muscle weakness, proximal, lower limbs" [OMIM:Muscle weakness, proximal, lower limbs]
OMIM: "Proximal muscle weakness in lower limbs" [OMIM:Proximal muscle weakness in lower limbs]
OMIM: "Lower limb muscle weakness, proximal" [OMIM:Lower limb muscle weakness, proximal]
Is a (Direct Parents):
HPO         Proximal 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)
                Proximal muscle weakness(HPO:0003701)
                   Proximal muscle weakness in lower limbs(HPO:0008994)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Emery-Dreifuss muscular dystrophy (Orphanet:98853)
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures (Orphanet:209341)
Autosomal dominant spastic paraplegia type 41 (Orphanet:320355)
Autosomal recessive limb girdle muscular dystrophy type 2A (Orphanet:267)
Autosomal recessive limb-girdle muscular dystrophy type 2G (Orphanet:34514)
Autosomal recessive limb-girdle muscular dystrophy type 2I (Orphanet:34515)
Becker muscular dystrophy (Orphanet:98895)
Duchenne muscular dystrophy (Orphanet:98896)
Proximal spinal muscular atrophy (Orphanet:70)
X-linked Emery-Dreifuss muscular dystrophy (Orphanet:98863)
X-linked myopathy with excessive autophagy (Orphanet:25980)