weakness
Basic Information
- Identifier
- SYMP_0000177
- Notation
- SYMP:0000177
- Category
- symptoms
Related Diseases
- 3-methylcrotonyl-CoA carboxylase 1 deficiency
- Arenaviridae infectious disease
- B acute lymphoblastic leukemia with DUX4 rearrangement
- Balkan nephropathy
- Balo concentric sclerosis
- Bartter disease
- Bartter disease type 3
- Bartter disease type 4b
- Blessig's cysts
- Brown-Sequard syndrome
- Brucella canis brucellosis
- Brucella melitensis brucellosis
- Brucella suis brucellosis
- COX deficiency, benign infantile mitochondrial myopathy
- Charcot-Marie-Tooth disease axonal type 2C
- Charcot-Marie-Tooth disease axonal type 2F
- Charcot-Marie-Tooth disease axonal type 2H
- Charcot-Marie-Tooth disease axonal type 2Q
- Charcot-Marie-Tooth disease axonal type 2T
- Charcot-Marie-Tooth disease axonal type 2U
- Charcot-Marie-Tooth disease axonal type 2X
- Charcot-Marie-Tooth disease type 1
- Charcot-Marie-Tooth disease type 2
- Charcot-Marie-Tooth disease type 2E
- Charcot-Marie-Tooth disease type 2I
- Charcot-Marie-Tooth disease type 2J
- Charcot-Marie-Tooth disease type 2R
- Charcot-Marie-Tooth disease, axonal type 2W
- Diamond-Blackfan anemia 16
- Diamond-Blackfan anemia 4
- Diamond-Blackfan anemia 5
- Diamond-blackfan anemia 3
- Ebola hemorrhagic fever
- Fanconi-like syndrome
- Finnish type amyloidosis
- GM2 gangliosidosis
- Gilbert syndrome
- Goodpasture syndrome
- IDH-mutant and 1p/19q-codeleted oligodendroglioma
- Murray Valley encephalitis
- Pancoast tumor
- Plasmodium vivax malaria
- Q fever
- Senior-Loken syndrome
- Venezuelan hemorrhagic fever
- Western equine encephalitis
- Yunis-Varon syndrome
- acquired polycythemia
- acute disseminated encephalomyelitis
- acute flaccid myelitis
- acute kidney failure
- acute leukemia
- acute myeloid leukemia with MLL rearrangement
- acute myeloid leukemia with t(6;9) (p23;q34.1)
- adrenal gland disease
- adult brain stem glioma
- adult central nervous system mature teratoma
- adult leptomeningeal melanoma
- adult oligodendroglioma
- amyotrophic lateral sclerosis
- amyotrophic lateral sclerosis type 12
- amyotrophic lateral sclerosis type 16
- amyotrophic lateral sclerosis type 18
- amyotrophic lateral sclerosis type 5
- amyotrophic lateral sclerosis type 9
- anaplastic astrocytoma
- angiodysplasia of intestine
- angiolipoma
- anhidrosis
- anuria
- aortic valve insufficiency
- astrocytoma, IDH-mutant, grade 4
- atherosclerosis
- atrial fibrillation
- atrial standstill 1
- atypical choroid plexus papilloma
- atypical chronic myeloid leukemia, BCR-ABL1 negative
- atypical hereditary sensory neuropathy
- autoimmune disease
- autoimmune disease of musculoskeletal system
- autoimmune disease of peripheral nervous system
- autoimmune polyendocrine syndrome
- autosomal dominant distal hereditary motor neuronopathy 10
- autosomal dominant limb-girdle muscular dystrophy type 2
- autosomal recessive distal hereditary motor neuronopathy 10
- autosomal recessive limb-girdle muscular dystrophy type 2M
- autosomal recessive limb-girdle muscular dystrophy type 2U
- babesiosis
- bagassosis
- baylisascariasis
- benign teratoma
- bone disease
- bone peripheral neuroepithelioma
- bone remodeling disease
- bone structure disease
- brachial plexus lesion
- brachial plexus neoplasm
- bradyopsia
- bradyopsia 2
- brain ependymoma
- brain oligodendroglioma
- brain stem astrocytic neoplasm
- brain stem infarction
- brucellosis
- cardiac arrest
- carpal tunnel syndrome
- carpal tunnel syndrome 1
- carpal tunnel syndrome 2
- cauda equina neoplasm
- cavernous hemangioma
- cellular ependymoma
- cellular schwannoma
- central nervous system benign neoplasm
- central nervous system disease
- central nervous system fibrosarcoma
- central nervous system neuroblastoma
- central nervous system origin vertigo
- central nervous system sarcoma
- centronuclear myopathy
- cerebral angioma
- cerebral cavernous malformation 3
- cerebral convexity meningioma
- cerebritis
- cervicomedullary junction neoplasm
- childhood leptomeningeal melanoma
- childhood spinal cord tumor
- childhood supratentorial embryonal tumor with multilayered rosettes, C19MC-altered
- cholesterol embolism
- chordoma
- chronic rapidly progressive glomerulonephritis
- clivus chondroid chordoma
- clivus chordoma
- colon mucinous adenocarcinoma
- combined oxidative phosphorylation deficiency 15
- congenital dyserythropoietic anemia
- congenital dyserythropoietic anemia type II
- congenital muscular dystrophy due to LMNA mutation
- congenital myasthenic syndrome
- congenital myasthenic syndrome 11
- congenital myasthenic syndrome 20
- congenital myasthenic syndrome 4C
- congenital myasthenic syndrome 5
- congenital myopathy 1B
- conus medullaris neoplasm
- conventional fibrosarcoma
- cranial nerve malignant neoplasm
- critical illness polyneuropathy
- cystic fibrosis
- cystinosis
- dermoid cyst of ovary
- desquamative interstitial pneumonia
- diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype
- digenic disease
- discitis
- dissociated nystagmus
- dropped head syndrome
- dumping syndrome
- dysbaric osteonecrosis
- dystonia 22, adult-onset
- dystransthyretinemic hyperthyroxinemia
- epicondylitis
- epidural spinal canal angiolipoma
- episodic ataxia type 7
- epithelial-myoepithelial carcinoma
- erythropoietin polycythemia
- essential thrombocythemia
- exfoliation syndrome
- exophthalmic ophthalmoplegia
- facioscapulohumeral muscular dystrophy 2
- familial hypocalciuric hypercalcemia 1
- familial hypocalciuric hypercalcemia 2
- familial juvenile hyperuricemic nephropathy
- femoral neuropathy
- fibroblastic liposarcoma
- frontal lobe neoplasm
- galactosemia
- gallbladder sarcoma
- giant axonal neuropathy 2
- giant cell glioblastoma
- glioblastoma classical subtype
- glioblastoma neural subtype
- hemangioblastoma
- hemangiopericytic tumor
- hemochromatosis type 2A
- hemochromatosis type 2B
- hemorrhagic disease
- hemosiderosis
- hepatitis B
- hepatoid adenocarcinoma
- hereditary sensory neuropathy type 1D
- hereditary sensory neuropathy type 1F
- hereditary spastic paraplegia 12
- hereditary spastic paraplegia 16
- hereditary spastic paraplegia 17
- hereditary spastic paraplegia 28
- hereditary spastic paraplegia 29
- hereditary spastic paraplegia 4
- hereditary spastic paraplegia 63
- hereditary spastic paraplegia 64
- hereditary spastic paraplegia 72A
- hereditary spastic paraplegia 77
- hereditary spastic paraplegia 81
- hereditary spastic paraplegia 87
- hereditary spastic paraplegia 90A
- hereditary spastic paraplegia 9B
- hexahydrophthalic anhydride allergic asthma
- histiocytic sarcoma
- histone mutated tumor
- hymenolepiasis
- hyperinsulinism
- hypertensive heart disease
- hypervalinemia and hyperleucine-isoleucinemia
- hypochromic microcytic anemia
- hypoglycemic coma
- hypoparathyroidism-deafness-renal disease syndrome
- hypoparathyroidism-retardation-dysmorphism syndrome
- hypophosphatemic nephrolithiasis/osteoporosis
- idiopathic scoliosis
- inflammatory and toxic neuropathy
- influenza
- insulinoma
- internuclear ophthalmoplegia
- intestinal hypomagnesemia 1
- intracranial berry aneurysm 4
- intracranial berry aneurysm 5
- intracranial meningioma
- intrinsic cardiomyopathy
- isolated anhidrosis with normal sweat glands
- isolated elevated serum creatine phosphokinase levels
- kyphosis
- lateral sclerosis
- leishmaniasis
- lesion of sciatic nerve
- liposarcoma
- long QT syndrome 4
- low grade glioma
- lung meningioma
- lung mucinous cystadenocarcinoma
- lymph node adenoid cystic carcinoma
- lymphoproliferative syndrome
- lymphoproliferative syndrome 2
- malignant adenoma
- malignant adult ependymoma
- malignant cardiac peripheral nerve sheath neoplasm
- malignant leptomeningeal neoplasm
- malignant melanocytic neoplasm of the peripheral nerve sheath
- malignant peripheral nerve sheath tumor
- medium chain acyl-CoA dehydrogenase deficiency
- medulloblastoma SHH activated
- medulloblastoma WNT activated
- medulloblastoma non-WNT/non-SHH group 3
- megaloblastic anemia
- melanotic medulloblastoma
- melanotic neurilemmoma
- meningeal melanocytoma
- meningioma
- mesenchymal chondrosarcoma
- metabolic dysfunction and alcohol associated liver disease
- metabolic dysfunction-associated steatotic liver disease
- methemoglobinemia
- microcystic meningioma
- mitochondrial complex I deficiency
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4A
- mixed-type liposarcoma
- mononeuritis of upper limb
- mononeuritis of upper limb and mononeuritis multiplex
- mononeuropathy
- multicentric Castleman disease
- musculoskeletal system disease
- myasthenia gravis
- nemaline myopathy 9
- nephronophthisis 2
- nerve compression syndrome
- nerve plexus neoplasm
- nerve root neoplasm
- neuroendocrine tumor
- neuromuscular disease
- neuromyelitis optica
- nocardiosis
- normocytic anemia
- notochordal cancer
- obsolete Coxiella burnetii pneumonia
- obsolete Ewing's family recurrent tumor
- obsolete Lymphocytic choriomeningitis virus meningitis
- obsolete adult meningioma
- obsolete adult rhabdomyosarcoma
- obsolete anaplastic childhood astrocytoma
- obsolete anosognostic epilepsy
- obsolete anthrax septicemia
- obsolete autosomal dominant limb-girdle muscular dystrophy type 1A
- obsolete benign glioma
- obsolete bovine anaplasmosis
- obsolete bovine tuberculosis
- obsolete calcium deposits in tendon and bursa
- obsolete candidal gastritis
- obsolete central nervous system hemangiopericytoma
- obsolete childhood supratentorial neoplasm
- obsolete congenital anemia
- obsolete deficiency anemia
- obsolete diabetes mellitus with hyperosmolarity
- obsolete disorder of magnesium metabolism
- obsolete distal hereditary motor neuronopathy type 5A
- obsolete endocrine tuberculosis
- obsolete enthesopathy of elbow
- obsolete equine infectious anemia
- obsolete heartwater disease
- obsolete hypoaldosteronism
- obsolete intestinal strongyloidiasis
- obsolete megakaryocytic tumor
- obsolete metastatic lung carcinoma
- obsolete neoplastic disease
- obsolete nontraumatic rupture of muscle
- obsolete peripheral neuropathy
- obsolete polyglandular activity in multiple endocrine adenomatosis
- obsolete precursor lymphoblastic lymphoma/leukemia
- obsolete primary Brucellaceae infectious disease
- obsolete primary Coxiellaceae infectious disease
- obsolete recurrent adult brain tumor
- obsolete recurrent childhood brainstem astrocytoma
- obsolete recurrent extrahepatic bile duct cancer
- obsolete relapsed meningioma
- obsolete secondary malignant neoplasm of lymph nodes of multiple site
- obsolete syphilitic pericarditis
- obsolete syringomyelia and syringobulbia
- obsolete tick paralysis
- obsolete yellow fever hepatitis
- oculopharyngodistal myopathy 2
- oligodendroglioma, IDH-mutant and 1p/19q-codeleted grade 2
- oligodendroglioma, IDH-mutant and 1p/19q-codeleted, grade 3
- osteochondritis dissecans
- ovarian lymphoma
- pancreatic acinar cell adenocarcinoma
- pancytopenia
- parathyroid gland benign neoplasm
- paratyphoid fever
- patellar tendinitis
- pericarditis
- peripheral artery disease
- peripheral nervous system neoplasm
- peroneal neuropathy
- plantar nerve lesion
- plexopathy
- polymyalgia rheumatica
- polymyositis
- polyneuropathy
- posterior foramen magnum meningioma
- postinfectious encephalitis
- primary diffuse large B-cell lymphoma of the central nervous system
- primary hypomagnesemia
- primary pigmented nodular adrenocortical disease
- primary pigmented nodular adrenocortical disease 2
- primary pigmented nodular adrenocortical disease 4
- pseudoxanthoma elasticum
- pyridoxine-responsive sideroblastic anemia
- rabies
- radial nerve lesion
- radial neuropathy
- radiculopathy
- rectum mucinous adenocarcinoma
- renal adenoma
- renal hypomagnesemia 3
- retinal hemangioblastoma
- retroperitoneal cancer
- rhabdoid cancer
- rhabdomyolysis-myalgia syndrome
- sacrum chordoma
- schwannomatosis
- schwannomatosis 1
- schwannomatosis 2
- scurvy
- secondary progressive multiple sclerosis
- sensory system cancer
- sepiapterin reductase deficiency
- short chain acyl-CoA dehydrogenase deficiency
- shoulder impingement syndrome
- sideroblastic anemia
- sideroblastic anemia 1
- sinusitis
- sleeping sickness
- somatoform disorder
- spastic ataxia 3
- spastic ataxia 4
- spinal canal and spinal cord meningioma
- spinal cord glioma
- spinal cord lipoma
- spinal cord lymphoma
- spinal cord melanoma
- spinocerebellar ataxia type 12
- splenic sequestration
- spondylolysis
- staphyloenterotoxemia
- sublingual gland adenoid cystic carcinoma
- sweat gland disease
- tanycytic ependymoma
- tethered spinal cord syndrome
- thalamic disease
- tibial neuropathy
- tick-borne encephalitis
- tooth resorption
- trench fever
- tubular aggregate myopathy 2
- typhoid fever
- uremic neuropathy
- variant ABeta2M amyloidosis
- vascular myelopathy
- vertebral artery insufficiency
- vestibular gland benign neoplasm
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It is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with questions about your medical condition.