Pelvic girdle muscle weakness

Symptom Information:

Symptom ID: HPO:0003749
Synonyms:
Hip girdle muscle weakness [HPO:0003749]
Hip girdle weakness [HPO:0003749]
Hip-girdle muscle weakness [HPO:0003749]
Pelvic girdle weakness [HPO:0003749]
Hip girdle muscle weakness [OMIM:Hip girdle muscle weakness]
Hip girdle weakness [OMIM:Hip girdle weakness]
Pelvic girdle muscle weakness [OMIM:Pelvic girdle muscle weakness]
Pelvic girdle weakness [OMIM:Pelvic girdle weakness]
Hip girdle muscle weakness (usually presenting symptom) [OMIM:Hip girdle muscle weakness (usually presenting symptom)]
Pelvic girdle muscle weakness (occurs earlier) [OMIM:Pelvic girdle muscle weakness (occurs earlier)]
Quality:
Cross references:
OMIM: "Hip girdle muscle weakness" [OMIM:Hip girdle muscle weakness]
OMIM: "Hip girdle weakness" [OMIM:Hip girdle weakness]
OMIM: "Pelvic girdle muscle weakness" [OMIM:Pelvic girdle muscle weakness]
OMIM: "Pelvic girdle weakness" [OMIM:Pelvic girdle weakness]
OMIM: "Hip girdle muscle weakness (usually presenting symptom)" [OMIM:Hip girdle muscle weakness (usually presenting symptom)]
OMIM: "Pelvic girdle muscle weakness (occurs earlier)" [OMIM:Pelvic girdle muscle weakness (occurs earlier)]
Is a (Direct Parents):
HPO         Limb-girdle muscle weakness
HPO         Abnormality of the hip-girdle musculature
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)
                Limb-girdle muscle weakness(HPO:0003325)
                   Pelvic girdle muscle weakness(HPO:0003749)
          Abnormality of the musculature of the pelvis(HPO:0001469)
             Abnormality of the hip-girdle musculature(HPO:0001445)
                Pelvic girdle muscle weakness(HPO:0003749)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

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)
Distal myopathy with early respiratory muscle involvement (Orphanet:34521)
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2 (OMIM:158901)
Glycogen storage disease due to phosphoglucomutase deficiency (Orphanet:711)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia (Orphanet:52430)
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers (Orphanet:206546)
X-linked Emery-Dreifuss muscular dystrophy (Orphanet:98863)