Progressive proximal muscle weakness

Symptom Information:

Symptom ID: HPO:0009073
Synonyms:
Muscle weakness, progressive, proximal [HPO:0009073]
Muscle weakness, progressive, proximal [OMIM:Muscle weakness, progressive, proximal]
Muscle weakness, proximal, progressive [OMIM:Muscle weakness, proximal, progressive]
Quality:
Cross references:
OMIM: "Muscle weakness, progressive, proximal" [OMIM:Muscle weakness, progressive, proximal]
OMIM: "Muscle weakness, proximal, progressive" [OMIM:Muscle weakness, proximal, progressive]
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)
                   Progressive proximal muscle weakness(HPO:0009073)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive limb-girdle muscular dystrophy type 2C (Orphanet:353)
MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET (OMIM:300718)
MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE (OMIM:300717)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT (OMIM:300695)
X-linked immunoneurologic disorder (Orphanet:2571)
X-linked myopathy with postural muscle atrophy (Orphanet:178461)
ZASP-related myofibrillar myopathy (Orphanet:98912)