Ragged-red muscle fibers
Symptom Information:
Symptom ID: | HPO:0003200 | |||||||
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 morphology(HPO:0011805) Abnormality of muscle fibers(HPO:0004303) Ragged-red muscle fibers(HPO:0003200) MedDRA: |
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Database Frequency: | 37 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
2p21 microdeletion syndrome | (Orphanet:163693) |
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | (Orphanet:329314) |
Atypical hypotonia - cystinuria syndrome | (Orphanet:238523) |
Autosomal dominant limb-girdle muscular dystrophy type 1H | (Orphanet:238755) |
Autosomal dominant optic atrophy and congenital deafness | (Orphanet:3212) |
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
COENZYME Q10 DEFICIENCY, PRIMARY, 1 | (OMIM:607426) |
Cardiomyopathy, familial hypertrophic, 8 | (OMIM:608751) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Fatal infantile lactic acidosis with methylmalonic aciduria | (Orphanet:17) |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |
Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
Isolated succinate-CoQ reductase deficiency | (Orphanet:3208) |
Kearns-Sayre syndrome | (Orphanet:480) |
Laing distal myopathy | (Orphanet:59135) |
Leber plus disease | (Orphanet:99718) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
MYASTHENIC SYNDROME, CONGENITAL, 14 | (OMIM:616228) |
MYOGLOBINURIA, RECURRENT | (OMIM:550500) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy | (Orphanet:255235) |
Mitochondrial DNA depletion syndrome, myopathic form | (Orphanet:254875) |
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | (Orphanet:254864) |
Mitochondrial neurogastrointestinal encephalomyopathy | (Orphanet:298) |
Myopathy and diabetes mellitus | (Orphanet:2596) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 2 | (OMIM:609283) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 | (OMIM:609286) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 5 | (OMIM:613077) |
Ramsay-Hunt syndrome | (Orphanet:3020) |
STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL | (OMIM:500003) |
Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |