Limb-girdle muscle weakness
Symptom Information:
Symptom ID: | HPO:0003325 | ||||||||
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) MedDRA: |
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Database Frequency: | 22 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | (Orphanet:329314) |
Alpha-crystallinopathy | (Orphanet:98910) |
Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
Autosomal recessive Emery-Dreifuss muscular dystrophy | (Orphanet:98855) |
Autosomal recessive limb girdle muscular dystrophy type 2A | (Orphanet:267) |
Autosomal recessive limb-girdle muscular dystrophy type 2D | (Orphanet:62) |
Autosomal recessive limb-girdle muscular dystrophy type 2E | (Orphanet:119) |
Autosomal recessive limb-girdle muscular dystrophy type 2F | (Orphanet:219) |
Autosomal recessive limb-girdle muscular dystrophy type 2K | (Orphanet:86812) |
Autosomal recessive limb-girdle muscular dystrophy type 2P | (Orphanet:280333) |
Becker muscular dystrophy | (Orphanet:98895) |
Bethlem myopathy | (Orphanet:610) |
Congenital muscular dystrophy type 1B | (Orphanet:98893) |
Diaphyseal medullary stenosis - bone malignancy | (Orphanet:85182) |
Distal myopathy, Nonaka type | (Orphanet:602) |
Duchenne muscular dystrophy | (Orphanet:98896) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
INCLUSION BODY MYOPATHY 2, AUTOSOMAL RECESSIVE | (OMIM:600737) |
MYASTHENIC SYNDROME, CONGENITAL, 14 | (OMIM:616228) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |