Limb muscle weakness
Symptom Information:
Symptom ID: | HPO:0003690 | ||||
Synonyms: |
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Quality: | |||||
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 muscle weakness(HPO:0003690) MedDRA: |
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Database Frequency: | 41 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Arnold-Chiari malformation type I | (Orphanet:268882) |
Arnold-Chiari malformation type II | (Orphanet:1136) |
Autosomal dominant Charcot-Marie-Tooth disease type 2O | (Orphanet:284232) |
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | (Orphanet:217055) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS | (OMIM:606842) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Charcot-Marie-Tooth disease type 4F | (Orphanet:99952) |
Choreoacanthocytosis | (Orphanet:2388) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
Diaphyseal medullary stenosis - bone malignancy | (Orphanet:85182) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
Glycogen storage disease due to acid maltase deficiency, infantile onset | (Orphanet:308552) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia | (Orphanet:52430) |
Kennedy disease | (Orphanet:481) |
MYASTHENIA GRAVIS | (OMIM:254200) |
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL | (OMIM:605809) |
Mitochondrial DNA depletion syndrome, myopathic form | (Orphanet:254875) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
NEMALINE MYOPATHY 4 | (OMIM:609285) |
NEMALINE MYOPATHY 6 | (OMIM:609273) |
Nemaline myopathy | (Orphanet:607) |
OCULAR MYOPATHY WITH CURARE SENSITIVITY | (OMIM:257600) |
Oculopharyngeal muscular dystrophy | (Orphanet:270) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 | (OMIM:157640) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 | (OMIM:609286) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 4 | (OMIM:610131) |
Primary CD59 deficiency | (Orphanet:169464) |
Primary basilar impression | (Orphanet:2285) |
REFSUM DISEASE, CLASSIC | (OMIM:266500) |
Refsum disease | (Orphanet:773) |
Spinal muscular atrophy with respiratory distress | (Orphanet:98920) |
Spinocerebellar ataxia type 18 | (Orphanet:98771) |
Spondyloepiphyseal dysplasia, Reardon type | (Orphanet:163662) |
Synaptic congenital myasthenic syndromes | (Orphanet:98915) |
Syringomyelia | (Orphanet:3280) |