Progressive muscle weakness

Symptom Information:

Symptom ID: HPO:0003323
Synonyms:
Muscle weakness, progressive [HPO:0003323]
Progressive muscular weakness [HPO:0003323]
Muscle weakness, progressive [OMIM:Muscle weakness, progressive]
Progressive muscle weakness [OMIM:Progressive muscle weakness]
Quality:
Cross references:
OMIM: "Muscle weakness, progressive" [OMIM:Muscle weakness, progressive]
OMIM: "Progressive muscle weakness" [OMIM:Progressive muscle weakness]
Is a (Direct Parents):
HPO         Muscle weakness
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:
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)