Generalized muscle weakness
Symptom Information:
Symptom ID: | HPO:0003324 | ||||||||||
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) Generalized muscle weakness(HPO:0003324) MedDRA: |
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Database Frequency: | 48 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Antenatal multiminicore disease with arthrogryposis multiplex congenita | (Orphanet:178148) |
Autosomal dominant hypophosphatemic rickets | (Orphanet:89937) |
Autosomal recessive limb-girdle muscular dystrophy type 2Q | (Orphanet:254361) |
BARTTER SYNDROME, ANTENATAL, TYPE 1 | (OMIM:601678) |
BARTTER SYNDROME, ANTENATAL, TYPE 2 | (OMIM:241200) |
Bartter syndrome | (Orphanet:112) |
Cap myopathy | (Orphanet:171881) |
Central core disease | (Orphanet:597) |
Classic Bartter syndrome | (Orphanet:93605) |
Classic multiminicore myopathy | (Orphanet:324604) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Congenital fiber-type disproportion myopathy | (Orphanet:2020) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Congenital muscular dystrophy with cerebellar involvement | (Orphanet:370959) |
Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
Desmin-related myopathy with Mallory body-like inclusions | (Orphanet:84132) |
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 2 | (OMIM:615539) |
Early-onset myopathy with fatal cardiomyopathy | (Orphanet:289377) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Gitelman syndrome | (Orphanet:358) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia | (Orphanet:79091) |
Infantile neuroaxonal dystrophy | (Orphanet:35069) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) | (OMIM:613662) |
MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEMATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS | (OMIM:601170) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 | (OMIM:253280) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 | (OMIM:613156) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 | (OMIM:606612) |
MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL | (OMIM:601462) |
MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL | (OMIM:608930) |
MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL | (OMIM:616321) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
MYOPATHY, MYOSIN STORAGE | (OMIM:608358) |
MYOPATHY, TUBULAR AGGREGATE, 2 | (OMIM:615883) |
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | (Orphanet:254864) |
Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
Moderate multiminicore disease with hand involvement | (Orphanet:178145) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A | (OMIM:256600) |
Nemaline myopathy | (Orphanet:607) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 2 | (OMIM:609283) |
Rigid spine syndrome | (Orphanet:97244) |
Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |
Steinert myotonic dystrophy | (Orphanet:273) |
Synaptic congenital myasthenic syndromes | (Orphanet:98915) |
X-linked centronuclear myopathy | (Orphanet:596) |