Progressive muscle weakness
Symptom Information:
Symptom ID: | HPO:0003323 | ||||
Synonyms: |
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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) Progressive muscle weakness(HPO:0003323) MedDRA: |
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Database Frequency: | 17 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
AMYOTROPHIC LATERAL SCLEROSIS 8 | (OMIM:608627) |
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
COENZYME Q10 DEFICIENCY, PRIMARY, 1 | (OMIM:607426) |
Glycogen storage disease due to acid maltase deficiency, infantile onset | (Orphanet:308552) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
Myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2 | (OMIM:613561) |
NARP syndrome | (Orphanet:644) |
NEMALINE MYOPATHY 5 | (OMIM:605355) |
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) |
Peripheral motor neuropathy - dysautonomia | (Orphanet:2400) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |