Pelvic girdle muscle weakness
Symptom Information:
Symptom ID: | HPO:0003749 | ||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |