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modern wellness · Symptom

Generalized muscle weakness

🩺 HPO Source

HPO ID

HPO Label

Generalized muscle weakness

HPO Definition

Generalized weakness or decreased strength of the muscles, affecting both distal and proximal musculature.

🔤 Synonyms (6)

Synonyms

Generalised muscle weaknessGeneralised weaknessGeneralized weaknessMuscle weakness, diffuseMuscle weakness, generalisedMuscle weakness, generalized

🔗 Cross-References (1)

UMLSC0746674

🔼 Broader Terms (1)

HP:0001324Muscle weakness

🏥 Conditions where Generalized muscle weakness appears

40 · bridged via HPO ↔ OMIM

syndrome OMIM 161800

Actin-Accumulation Myopathy

syndrome OMIM 193100

Autosomal Dominant Hypophosphatemic Rickets

syndrome OMIM 241200

Bartter Syndrome, Antenatal , Type 2

syndrome OMIM 601678

Bartter Syndrome, Antenatal Type 1

syndrome OMIM 607364

Bartter Syndrome, Type 3

syndrome OMIM 607364

Bartter Syndrome, Type 3, With Hypocalciuria

syndrome OMIM 211530

Brown-Vialetto-Van Laere Syndrome 1

freq: 1/9 ev: PCS

syndrome OMIM 212350

Cataract And Cardiomyopathy

freq: 1/2 ev: PCS

syndrome OMIM 117000

Central Core Myopathy (Disorder)

syndrome OMIM 614096

Combined Oxidative Phosphorylation Deficiency 8

freq: 1/2 ev: PCS

disease OMIM 255310

Congenital Fiber Type Disproportion

syndrome OMIM 606703

Dyskinesia, Familial, With Facial Myokymia

freq: 1/2 ev: PCS

syndrome OMIM 615539

Ehlers-Danlos Syndrome, Musculocontractural Type, 2

freq: 1/1 ev: PCS

syndrome OMIM 602771

Eichsfeld Type Congenital Muscular Dystrophy

syndrome OMIM 603034

Endplate Acetylcholinesterase Deficiency (Disorder)

freq: 1/6 ev: PCS

syndrome OMIM 263800

Gitelman Syndrome

syndrome OMIM 154020

Hypomagnesemia 2, Renal

syndrome OMIM 605637

Inclusion Body Myopathy 3, Autosomal Dominant

syndrome OMIM 256600

Infantile Neuroaxonal Dystrophy

syndrome OMIM 613327

Lipodystrophy, Congenital Generalized, Type 4

syndrome OMIM 255320

Minicore Myopathy With External Ophthalmoplegia (Disorder)

freq: 1/1 ev: PCS

syndrome OMIM 613662

Mitochondrial Dna Depletion Syndrome 4B (Mngie Type)

syndrome OMIM 117000

Multiminicore Disease, Moderate, With Hand Involvement

syndrome OMIM 615330

Multiple Mitochondrial Dysfunctions Syndrome 3

freq: 1/2 ev: PCS

syndrome OMIM 253280

Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 3

syndrome OMIM 613156

Muscular Dystrophy-Dystroglycanopathy (Congenital With Mental Retardation), Type B, 2

freq: 14/14 ev: PCS

syndrome OMIM 613152

Muscular Dystrophy-Dystroglycanopathy (Congenital Without Mental Retardation), Type B, 4

freq: 1/1 ev: PCS

syndrome OMIM 606612

Muscular Dystrophy, Congenital, 1C

freq: 9/9 ev: PCS

syndrome OMIM 613723

Muscular Dystrophy, Limb-Girdle, Type 2Q

syndrome OMIM 616326

Myasthenic Syndrome, Congenital, 11, Associated With Acetylcholine Receptor Deficiency

freq: 1/4 ev: PCS

syndrome OMIM 601462

Myasthenic Syndrome, Congenital, 1A, Slow-Channel

freq: 2/4 ev: PCS

syndrome OMIM 608930

Myasthenic Syndrome, Congenital, 1B, Fast-Channel

syndrome OMIM 616321

Myasthenic Syndrome, Congenital, 3A, Slow-Channel

freq: 1/1 ev: PCS

syndrome OMIM 616325

Myasthenic Syndrome, Congenital, 9, Associated With Acetylcholine Receptor Deficiency

freq: 1/1 ev: PCS

syndrome OMIM 161800

Myopathy, Actin, Congenital, With Cores

syndrome OMIM 161800

Myopathy, Actin, Congenital, With Excess of Thin Myofilaments

syndrome OMIM 611705

Myopathy, Early-Onset, With Fatal Cardiomyopathy

freq: 5/5 ev: PCS

syndrome OMIM 612954

Myopathy, Myofibrillar, Bag3-Related

freq: 1/3 ev: PCS

syndrome OMIM 608358

Myopathy, Myosin Storage (Disorder)

syndrome OMIM 615883

Myopathy, Tubular Aggregate, 2

freq: 5/6 ev: PCS