Generalized muscle weakness

Symptom Information:

Symptom ID: HPO:0003324
Synonyms:
Generalized weakness [HPO:0003324]
Muscle weakness, diffuse [HPO:0003324]
Muscle weakness, generalized [HPO:0003324]
Generalized muscle weakness [OMIM:Generalized muscle weakness]
Generalized weakness [OMIM:Generalized weakness]
Muscle weakness, diffuse [OMIM:Muscle weakness, diffuse]
Muscle weakness, generalized [OMIM:Muscle weakness, generalized]
Generalized muscle weakness (less common) [OMIM:Generalized muscle weakness (less common)]
Generalized weakness (adult-onset) [OMIM:Generalized weakness (adult-onset)]
Weakness, generalized [OMIM:Weakness, generalized]
Quality:
Cross references:
OMIM: "Generalized muscle weakness" [OMIM:Generalized muscle weakness]
OMIM: "Generalized weakness" [OMIM:Generalized weakness]
OMIM: "Muscle weakness, diffuse" [OMIM:Muscle weakness, diffuse]
OMIM: "Muscle weakness, generalized" [OMIM:Muscle weakness, generalized]
OMIM: "Generalized muscle weakness (less common)" [OMIM:Generalized muscle weakness (less common)]
OMIM: "Generalized weakness (adult-onset)" [OMIM:Generalized weakness (adult-onset)]
OMIM: "Weakness, generalized" [OMIM:Weakness, generalized]
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)
                Generalized muscle weakness(HPO:0003324)
MedDRA:
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)