Shoulder girdle muscle weakness

Symptom Information:

Symptom ID: HPO:0003547
Synonyms:
Muscle weakness, shoulder-girdle [HPO:0003547]
Shoulder girdle weakness [HPO:0003547]
Shoulder weakness [HPO:0003547]
Muscle weakness, shoulder-girdle [OMIM:Muscle weakness, shoulder-girdle]
Shoulder girdle muscle weakness [OMIM:Shoulder girdle muscle weakness]
Shoulder girdle weakness [OMIM:Shoulder girdle weakness]
Shoulder weakness [OMIM:Shoulder weakness]
Quality:
Cross references:
OMIM: "Muscle weakness, shoulder-girdle" [OMIM:Muscle weakness, shoulder-girdle]
OMIM: "Shoulder girdle muscle weakness" [OMIM:Shoulder girdle muscle weakness]
OMIM: "Shoulder girdle weakness" [OMIM:Shoulder girdle weakness]
OMIM: "Shoulder weakness" [OMIM:Shoulder weakness]
Is a (Direct Parents):
HPO         Abnormality of the shoulder girdle musculature
HPO         Limb-girdle muscle weakness
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the musculature of the limbs(HPO:0009127)
                      Abnormality of the musculature of the upper limbs(HPO:0001446)
                         Abnormality of the shoulder girdle musculature(HPO:0001435)
                            Shoulder girdle muscle weakness(HPO:0003547)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Muscle weakness(HPO:0001324)
                Limb-girdle muscle weakness(HPO:0003325)
                   Shoulder girdle muscle weakness(HPO:0003547)
          Abnormality of the musculature of the limbs(HPO:0009127)
             Abnormality of the musculature of the upper limbs(HPO:0001446)
                Abnormality of the shoulder girdle musculature(HPO:0001435)
                   Shoulder girdle muscle weakness(HPO:0003547)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Emery-Dreifuss muscular dystrophy (Orphanet:98853)
Autosomal dominant limb-girdle muscular dystrophy type 1A (Orphanet:266)
Autosomal dominant limb-girdle muscular dystrophy type 1B (Orphanet:264)
Autosomal dominant limb-girdle muscular dystrophy type 1D (Orphanet:34516)
Autosomal dominant limb-girdle muscular dystrophy type 1F (Orphanet:55595)
Autosomal dominant limb-girdle muscular dystrophy type 1G (Orphanet:55596)
Autosomal recessive Emery-Dreifuss muscular dystrophy (Orphanet:98855)
Autosomal recessive limb-girdle muscular dystrophy type 2H (Orphanet:1878)
Autosomal recessive limb-girdle muscular dystrophy type 2I (Orphanet:34515)
Autosomal recessive limb-girdle muscular dystrophy type 2L (Orphanet:206549)
Congenital muscular dystrophy type 1B (Orphanet:98893)
Congenital muscular dystrophy with cerebellar involvement (Orphanet:370959)
Distal myopathy with early respiratory muscle involvement (Orphanet:34521)
Distal myopathy with vocal cord weakness (Orphanet:600)
Duchenne muscular dystrophy (Orphanet:98896)
Facioscapulohumeral dystrophy (Orphanet:269)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia (Orphanet:52430)
MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE (OMIM:609456)
MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL (OMIM:310095)
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers (Orphanet:206546)
VACUOLAR NEUROMYOPATHY (OMIM:601846)