muscle weakness
Basic Information
- Identifier
- SYMP_0000094
- Notation
- SYMP:0000094
- Category
- symptoms
Related Diseases
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- 3-methylcrotonyl-CoA carboxylase deficiency
- 3-methylglutaconic aciduria type 5
- ACTH-independent macronodular adrenal hyperplasia
- ACTH-independent macronodular adrenal hyperplasia 1
- ACTH-independent macronodular adrenal hyperplasia 2
- AGAT deficiency
- Addison's disease
- Andersen-Tawil syndrome
- BH4-deficient hyperphenylalaninemia D
- Barth syndrome
- Bartter disease type 1
- Bartter disease type 3
- Bartter disease type 5
- Becker disease
- Becker muscular dystrophy
- Bethlem myopathy
- Brown-Vialetto-Van Laere syndrome 2
- CK syndrome
- COX deficiency, infantile mitochondrial myopathy
- Camurati-Engelmann disease
- Charcot-Marie-Tooth disease
- Charcot-Marie-Tooth disease X-linked recessive 3
- Charcot-Marie-Tooth disease X-linked recessive 4
- Charcot-Marie-Tooth disease axonal type 2CC
- Charcot-Marie-Tooth disease axonal type 2K
- Charcot-Marie-Tooth disease dominant intermediate B
- Charcot-Marie-Tooth disease dominant intermediate F
- Charcot-Marie-Tooth disease intermediate type
- Charcot-Marie-Tooth disease recessive intermediate D
- Charcot-Marie-Tooth disease type 1B
- Charcot-Marie-Tooth disease type 1C
- Charcot-Marie-Tooth disease type 1E
- Charcot-Marie-Tooth disease type 1F
- Charcot-Marie-Tooth disease type 1G
- Charcot-Marie-Tooth disease type 2A2B
- Charcot-Marie-Tooth disease type 2B
- Charcot-Marie-Tooth disease type 2B1
- Charcot-Marie-Tooth disease type 2E
- Charcot-Marie-Tooth disease type 2I
- Charcot-Marie-Tooth disease type 2J
- Charcot-Marie-Tooth disease type 2Y
- Charcot-Marie-Tooth disease type 3
- Charcot-Marie-Tooth disease type 4
- Charcot-Marie-Tooth disease type 4A
- Charcot-Marie-Tooth disease type 4B1
- Charcot-Marie-Tooth disease type 4B2
- Charcot-Marie-Tooth disease type 4F
- Charcot-Marie-Tooth disease type 4J
- Charcot-Marie-Tooth disease type 4K
- Charcot-Marie-Tooth disease type 6
- Compton-North congenital myopathy
- Conn's syndrome
- Duchenne muscular dystrophy
- Ebola hemorrhagic fever
- Ehlers-Danlos syndrome classic-like 1
- Ehlers-Danlos syndrome musculocontractural type 1
- Ehlers-Danlos syndrome musculocontractural type 2
- Ehlers-Danlos syndrome spondylodysplastic type 3
- Fanconi renotubular syndrome 1
- Fanconi renotubular syndrome 2
- Fanconi renotubular syndrome 4
- Fanconi renotubular syndrome 5
- Fanconi syndrome
- Fanconi-like syndrome
- Friedreich ataxia 1
- Fukuyama congenital muscular dystrophy
- GM1 gangliosidosis type 1
- GM2 gangliosidosis
- GNE myopathy
- Guillain-Barre syndrome
- Hirata disease
- IDH-wildtype glioblastoma
- Koolen de Vries syndrome
- Krabbe disease
- Lambert-Eaton myasthenic syndrome
- Leber plus disease
- MELAS syndrome
- MERRF syndrome
- Marinesco-Sjogren syndrome
- Miyoshi muscular dystrophy
- Miyoshi muscular dystrophy 1
- Miyoshi muscular dystrophy 2
- Moebius syndrome
- NARP syndrome
- Native American myopathy
- PEHO syndrome
- Pearson syndrome
- Plummer's disease
- Sandhoff disease
- Schindler disease type 1
- Schmid metaphyseal chondrodysplasia
- Schwartz-Jampel syndrome 1
- Tay-Sachs disease
- Troyer syndrome
- Ullrich congenital muscular dystrophy
- Ullrich congenital muscular dystrophy 1A
- Ullrich congenital muscular dystrophy 1B
- Ullrich congenital muscular dystrophy 1C
- Ullrich congenital muscular dystrophy 2
- Unverricht-Lundborg syndrome
- Walker-Warburg syndrome
- Warburg micro syndrome 2
- Werdnig-Hoffmann disease
- West Nile encephalitis
- X-linked Emery-Dreifuss muscular dystrophy 1
- X-linked Emery-Dreifuss muscular dystrophy 6
- X-linked congenital myopathy with fiber-type disproportion
- X-linked distal spinal muscular atrophy 3
- X-linked dominant hypophosphatemic rickets
- X-linked myopathy with excessive autophagy
- X-linked recessive hypophosphatemic rickets
- X-linked spinocerebellar ataxia 2
- X-linked spinocerebellar ataxia 4
- X-linked spinocerebellar ataxia 5
- Y-linked spermatogenic failure 1
- Zika virus congenital syndrome
- acquired generalized lipodystrophy
- acute cholangitis
- adrenal cortex cancer
- adrenal cortex disease
- adrenal cortical adenoma
- adrenocortical carcinoma
- adult hypophosphatasia
- adult spinal muscular atrophy
- adult-onset ataxia and polyneuropathy
- adult-onset autosomal dominant demyelinating leukodystrophy
- alcoholic neuropathy
- amyotrophic lateral sclerosis type 1
- amyotrophic lateral sclerosis type 11
- amyotrophic lateral sclerosis type 12
- amyotrophic lateral sclerosis type 15
- amyotrophic lateral sclerosis type 19
- amyotrophic lateral sclerosis type 24
- amyotrophic lateral sclerosis type 25
- amyotrophic lateral sclerosis type 3
- amyotrophic lateral sclerosis type 8
- amyotrophic lateral sclerosis-parkinsonism/dementia complex 1
- amyotrophic neuralgia
- antisynthetase syndrome
- arthrogryposis multiplex congenita
- arthrogryposis multiplex congenita-1
- arthrogryposis multiplex congenita-3
- aspirin-induced respiratory disease
- ataxia telangiectasia
- autoimmune disease of musculoskeletal system
- autoimmune neuropathy
- autoimmune peripheral neuropathy
- autosomal dominant Emery-Dreifuss muscular dystrophy 5
- autosomal dominant Emery-Dreifuss muscular dystrophy 7
- autosomal dominant adult-onset proximal spinal muscular atrophy
- autosomal dominant distal hereditary motor neuronopathy 1
- autosomal dominant distal hereditary motor neuronopathy 10
- autosomal dominant distal hereditary motor neuronopathy 2
- autosomal dominant distal hereditary motor neuronopathy 3
- autosomal dominant distal hereditary motor neuronopathy 4
- autosomal dominant distal hereditary motor neuronopathy 5
- autosomal dominant distal hereditary motor neuronopathy 6
- autosomal dominant distal hereditary motor neuronopathy 7
- autosomal dominant distal hereditary motor neuronopathy 8
- autosomal dominant distal hereditary motor neuronopathy 9
- autosomal dominant hyaline body myopathy
- autosomal dominant hypocalcemia 2
- autosomal dominant limb-girdle muscular dystrophy type 1H
- autosomal dominant progressive external ophthalmoplegia 1
- autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
- autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6
- autosomal recessive centronuclear myopathy
- autosomal recessive cutis laxa type IIIA
- autosomal recessive distal hereditary motor neuronopathy 1
- autosomal recessive distal hereditary motor neuronopathy 2
- autosomal recessive distal hereditary motor neuronopathy 3
- autosomal recessive distal hereditary motor neuronopathy 4
- autosomal recessive distal hereditary motor neuronopathy 5
- autosomal recessive distal hereditary motor neuronopathy 7
- autosomal recessive hyaline body myopathy
- autosomal recessive hypophosphatemic rickets
- autosomal recessive limb-girdle muscular dystrophy type 2E
- autosomal recessive limb-girdle muscular dystrophy type 2G
- autosomal recessive limb-girdle muscular dystrophy type 2H
- autosomal recessive limb-girdle muscular dystrophy type 2M
- autosomal recessive limb-girdle muscular dystrophy type 2N
- autosomal recessive limb-girdle muscular dystrophy type 2Q
- autosomal recessive limb-girdle muscular dystrophy type 2W
- autosomal recessive limb-girdle muscular dystrophy type 2Z
- autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2
- autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3
- autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4
- autosomal recessive spinocerebellar ataxia 2
- axial osteomalacia
- bone deterioration disease
- carnitine-acylcarnitine translocase deficiency
- centronuclear myopathy 1
- centronuclear myopathy 2
- centronuclear myopathy 5
- centronuclear myopathy 6 with fiber-type disproportion
- chromosome 15q26-qter deletion syndrome
- chromosome Xp21 deletion syndrome
- chronic inflammatory demyelinating polyneuritis
- chronic inflammatory demyelinating polyradiculoneuropathy
- chronic polyneuropathy
- combined oxidative phosphorylation deficiency 1
- combined oxidative phosphorylation deficiency 13
- combined oxidative phosphorylation deficiency 22
- combined oxidative phosphorylation deficiency 26
- combined oxidative phosphorylation deficiency 33
- combined oxidative phosphorylation deficiency 34
- combined oxidative phosphorylation deficiency 36
- combined oxidative phosphorylation deficiency 4
- combined oxidative phosphorylation deficiency 49
- combined oxidative phosphorylation deficiency 55
- combined oxidative phosphorylation deficiency 6
- complete generalized lipodystrophy
- congenital disorder of glycosylation Ia
- congenital disorder of glycosylation Iaa
- congenital disorder of glycosylation Ic
- congenital disorder of glycosylation Id
- congenital disorder of glycosylation If
- congenital disorder of glycosylation Ig
- congenital disorder of glycosylation Ii
- congenital disorder of glycosylation Ik
- congenital disorder of glycosylation Il
- congenital disorder of glycosylation Im
- congenital disorder of glycosylation In
- congenital disorder of glycosylation Ip
- congenital disorder of glycosylation Ir
- congenital disorder of glycosylation It
- congenital disorder of glycosylation Iw
- congenital disorder of glycosylation Iy
- congenital disorder of glycosylation type I
- congenital disorder of glycosylation type II
- congenital disorder of glycosylation type IIb
- congenital disorder of glycosylation type IIc
- congenital disorder of glycosylation type IIf
- congenital disorder of glycosylation type IIl
- congenital disorder of glycosylation type IIm
- congenital disorder of glycosylation type IIn
- congenital disorder of glycosylation type IIo
- congenital disorder of glycosylation type IIp
- congenital generalized lipodystrophy type 4
- congenital glutamine deficiency
- congenital merosin-deficient muscular dystrophy 1A
- congenital muscular dystrophy
- congenital muscular dystrophy 1B
- congenital muscular dystrophy due to LMNA mutation
- congenital muscular dystrophy due to integrin alpha-7 deficiency
- congenital muscular dystrophy with cataracts and intellectual disability
- congenital muscular dystrophy-dystroglycanopathy A14
- congenital muscular dystrophy-dystroglycanopathy type A
- congenital muscular dystrophy-dystroglycanopathy type A2
- congenital muscular dystrophy-dystroglycanopathy type A6
- congenital myasthenic syndrome
- congenital myasthenic syndrome 10
- congenital myasthenic syndrome 11
- congenital myasthenic syndrome 12
- congenital myasthenic syndrome 13
- congenital myasthenic syndrome 14
- congenital myasthenic syndrome 15
- congenital myasthenic syndrome 16
- congenital myasthenic syndrome 17
- congenital myasthenic syndrome 18
- congenital myasthenic syndrome 19
- congenital myasthenic syndrome 1A
- congenital myasthenic syndrome 1B
- congenital myasthenic syndrome 22
- congenital myasthenic syndrome 2A
- congenital myasthenic syndrome 2C
- congenital myasthenic syndrome 3A
- congenital myasthenic syndrome 3B
- congenital myasthenic syndrome 3C
- congenital myasthenic syndrome 4A
- congenital myasthenic syndrome 4B
- congenital myasthenic syndrome 4C
- congenital myasthenic syndrome 6
- congenital myasthenic syndrome 7
- congenital myasthenic syndrome 8
- congenital myasthenic syndrome 9
- congenital myopathy
- congenital myopathy 10B
- congenital myopathy 14
- congenital myopathy 16
- congenital myopathy 17
- congenital myopathy 18
- congenital myopathy 20
- congenital myopathy 21
- congenital myopathy 22A
- congenital myopathy 22B
- congenital myopathy 2B
- congenital myopathy 2C
- congenital myopathy 6
- congenital myopathy 9A
- congenital myopathy 9B
- conversion disorder
- cranial nerve malignant neoplasm
- cylindrical spirals myopathy
- demyelinating disease
- demyelinating polyneuropathy
- dermatomyositis
- developmental delay, dysmorphic facies, and brain anomalies
- developmental delay, hypotrophy, and dysmorphic features without Moebius syndrome
- diabetic encephalopathy
- dimethylglycine dehydrogenase deficiency
- disease of metabolism
- distal arthrogryposis
- distal arthrogryposis type 2B3
- distal myopathy
- distal myopathy 1
- distal myopathy 3
- distal myopathy 4
- distal myopathy with rimmed vacuoles
- early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome
- epidermolysis bullosa simplex with muscular dystrophy
- episodic ataxia type 4
- episodic ataxia type 5
- episodic ataxia type 7
- episodic ataxia type 8
- facioscapulohumeral muscular dystrophy 2
- familial expansile osteolysis
- familial hemiplegic migraine
- familial isolated deficiency of vitamin E
- familial isolated hypoparathyroidism
- familial partial lipodystrophy
- fatal infantile hypertonic myofibrillar myopathy
- fibular hypoplasia and complex brachydactyly
- frontotemporal dementia
- gangliosidosis
- giant axonal neuropathy 1
- giant axonal neuropathy 2
- glucocorticoid-induced osteoporosis
- glucocorticoid-remediable aldosteronism
- glutamate formiminotransferase deficiency
- glycogen storage disease I
- glycogen storage disease II
- glycogen storage disease III
- glycogen storage disease IV
- glycogen storage disease IXd
- glycogen storage disease Ic
- glycogen storage disease VII
- glycogen storage disease XV
- growth hormone secreting pituitary adenoma
- hemiplegia
- hereditary hypophosphatemic rickets with hypercalciuria
- hereditary neuropathy with liability to pressure palsies
- hereditary sensory and autonomic neuropathy type 7
- hereditary spastic paraplegia 15
- hereditary spastic paraplegia 16
- hereditary spastic paraplegia 25
- hereditary spastic paraplegia 3A
- hereditary spastic paraplegia 4
- hereditary spastic paraplegia 43
- hereditary spastic paraplegia 47
- hereditary spastic paraplegia 49
- hereditary spastic paraplegia 50
- hereditary spastic paraplegia 5A
- hereditary spastic paraplegia 64
- hereditary spastic paraplegia 70
- hereditary spastic paraplegia 78
- herpes zoster
- holoprosencephaly 7
- hyaline body myopathy
- hypercalcemia
- hyperkalemic periodic paralysis
- hyperparathyroidism
- hyperphosphatasia with impaired intellectual development syndrome 3
- hyperphosphatasia with impaired intellectual development syndrome 5
- hyperthyroidism
- hypogonadotropic hypogonadism 8 with or without anosmia
- hypokalemia
- hypokalemic periodic paralysis
- hypomyelinating leukodystrophy 24
- hypophosphatemia
- hypophosphatemic nephrolithiasis/osteoporosis
- hypophosphatemic nephrolithiasis/osteoporosis 2
- hypothyroidism
- idiopathic progressive polyneuropathy
- impotence
- inappropriate ADH syndrome
- inclusion body myopathy and brain white matter abnormalities
- inclusion body myopathy with Paget disease of bone and frontotemporal dementia
- inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
- inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2
- inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3
- inclusion body myositis
- infant botulism
- integumentary system disease
- intermediate spinal muscular atrophy
- intestinal hypomagnesemia 1
- intracranial berry aneurysm 10
- intrinsic cardiomyopathy
- isolated elevated serum creatine phosphokinase levels
- juvenile amyotrophic lateral sclerosis type 27
- juvenile amyotrophic lateral sclerosis with dementia
- juvenile spinal muscular atrophy
- lateral sclerosis
- limb-girdle muscular dystrophy
- lysinuric protein intolerance
- malignant adenoma
- megaconial type congenital muscular dystrophy
- megaloblastic anemia
- meningovascular neurosyphilis
- methylmalonic acidemia due to transcobalamin receptor defect
- mineral metabolism disease
- mitochondrial DNA depletion syndrome 11
- mitochondrial DNA depletion syndrome 12b
- mitochondrial DNA depletion syndrome 13
- mitochondrial DNA depletion syndrome 14
- mitochondrial DNA depletion syndrome 16B
- mitochondrial DNA depletion syndrome 18
- mitochondrial DNA depletion syndrome 19
- mitochondrial DNA depletion syndrome 2
- mitochondrial DNA depletion syndrome 4b
- mitochondrial DNA depletion syndrome 8a
- mitochondrial DNA depletion syndrome 9
- mitochondrial complex III deficiency nuclear type 1
- mitochondrial complex III deficiency nuclear type 3
- mitochondrial complex III deficiency nuclear type 4
- mitochondrial complex III deficiency nuclear type 5
- mitochondrial complex III deficiency nuclear type 9
- mitochondrial complex IV deficiency nuclear type 13
- mitochondrial complex IV deficiency nuclear type 14
- mitochondrial complex IV deficiency nuclear type 17
- mitochondrial complex IV deficiency nuclear type 18
- mitochondrial complex IV deficiency nuclear type 19
- mitochondrial complex IV deficiency nuclear type 3
- mitochondrial complex V (ATP synthase) deficiency
- mitochondrial type mitochondrial complex I deficiency 1
- mixed connective tissue disease
- motor neuron disease
- mucopolysaccharidosis IVA
- mucosulfatidosis
- multiple acyl-CoA dehydrogenase deficiency
- multiple endocrine neoplasia type 1
- multiple mitochondrial dysfunctions syndrome 1
- multiple mitochondrial dysfunctions syndrome 2
- multiple mitochondrial dysfunctions syndrome 4
- multiple sclerosis
- multisystem proteinopathy
- muscle benign neoplasm
- muscular disease
- muscular dystrophy
- muscular dystrophy-dystroglycanopathy
- muscular dystrophy-dystroglycanopathy type B
- muscular dystrophy-dystroglycanopathy type B1
- muscular dystrophy-dystroglycanopathy type B2
- muscular dystrophy-dystroglycanopathy type B4
- muscular dystrophy-dystroglycanopathy type C8
- mutism
- myasthenia gravis
- myelitis
- myoepithelial carcinoma
- myofibrillar myopathy
- myofibrillar myopathy 1
- myofibrillar myopathy 10
- myofibrillar myopathy 11
- myofibrillar myopathy 4
- myofibrillar myopathy 5
- myofibrillar myopathy 6
- myofibrillar myopathy 7
- myofibrillar myopathy 8
- myofibrillar myopathy 9
- myopathy
- myopathy with extrapyramidal signs
- myopathy, lactic acidosis, and sideroblastic anemia 1
- myopathy, lactic acidosis, and sideroblastic anemia 2
- myopathy, lactic acidosis, and sideroblastic anemia 3
- myositis
- myotonia congenita
- myotonic disease
- myotonic dystrophy type 1
- myotonic dystrophy type 2
- narcolepsy
- nemaline myopathy
- nemaline myopathy 1
- nemaline myopathy 10
- nemaline myopathy 11
- nemaline myopathy 3
- nemaline myopathy 4
- nemaline myopathy 5B
- nemaline myopathy 5C
- nemaline myopathy 6
- nemaline myopathy 7
- nemaline myopathy 8
- nemaline myopathy 9
- neuroacanthocytosis
- neurodegenerative disease
- neurofibromatosis-Noonan syndrome
- neurogenic scapuloperoneal syndrome Kaeser type
- neurohypophyseal diabetes insipidus
- neuromuscular disease
- neuropathy
- neuroschistosomiasis
- nodular goiter
- non-severe COVID-19
- nuclear type mitochondrial complex I deficiency
- nuclear type mitochondrial complex I deficiency 1
- nuclear type mitochondrial complex I deficiency 11
- nuclear type mitochondrial complex I deficiency 14
- nuclear type mitochondrial complex I deficiency 16
- nuclear type mitochondrial complex I deficiency 17
- nuclear type mitochondrial complex I deficiency 18
- nuclear type mitochondrial complex I deficiency 19
- nuclear type mitochondrial complex I deficiency 20
- nuclear type mitochondrial complex I deficiency 22
- nuclear type mitochondrial complex I deficiency 23
- nuclear type mitochondrial complex I deficiency 25
- nuclear type mitochondrial complex I deficiency 26
- nuclear type mitochondrial complex I deficiency 27
- nuclear type mitochondrial complex I deficiency 31
- nuclear type mitochondrial complex I deficiency 32
- nuclear type mitochondrial complex I deficiency 33
- nuclear type mitochondrial complex I deficiency 34
- nuclear type mitochondrial complex I deficiency 4
- nuclear type mitochondrial complex I deficiency 9
- nutritional deficiency disease
- obsolete Charcot-Marie-Tooth disease axonal type 2G
- obsolete Pyles dysplasia
- obsolete X-linked sensorineural deafness
- obsolete amyotrophic lateral sclerosis type 17
- obsolete ascorbic acid deficiency
- obsolete atonic epilepsy
- obsolete autosomal dominant limb-girdle muscular dystrophy type 1A
- obsolete autosomal recessive limb-girdle muscular dystrophy type 2R
- obsolete candidal meningitis
- obsolete carbohydrate metabolism disease
- obsolete chronic progressive multiple sclerosis
- obsolete distal hereditary motor neuronopathy type 2A
- obsolete distal hereditary motor neuronopathy type 5A
- obsolete distal hereditary motor neuronopathy type 7A
- obsolete drug-Induced dyskinesia
- obsolete equine infectious anemia
- obsolete familial hypophosphatemia
- obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum
- obsolete influenza myositis
- obsolete lung carcinoma metastatic to the brain
- obsolete magnesium deficiency
- obsolete mannosidase deficiency disease
- obsolete metastatic ovarian small cell carcinoma with hypercalcemia
- obsolete mitochondrial disease
- obsolete non-toxic nodular goiter
- obsolete nontraumatic rupture of muscle
- obsolete peripheral neuropathy
- obsolete polioencephalitis
- obsolete pulmonary syphilis
- obsolete secondary malignant neoplasm of brain and spinal cord
- obsolete secondary thyroid hyperplasia
- obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
- obsolete syringomyelia and syringobulbia
- obsolete vitamin D deficiency
- oculopharyngodistal myopathy 1
- organic acidemia
- osteogenesis imperfecta type 10
- osteogenesis imperfecta type 12
- osteogenesis imperfecta type 15
- osteogenesis imperfecta type 4
- osteogenesis imperfecta type 5
- osteogenesis imperfecta type 6
- osteogenesis imperfecta type 8
- osteomalacia
- pancreatic agenesis
- paralytic poliomyelitis
- paramyotonia congenita of Von Eulenburg
- parathyroid gland benign neoplasm
- parathyroid gland disease
- peripartum cardiomyopathy
- peroxisome biogenesis disorder 7A
- phosphoglycerate kinase 1 deficiency
- phosphorus metabolism disease
- pigmented villonodular synovitis
- pituitary cancer
- polygenic disease
- polymyositis
- pontocerebellar hypoplasia type 8
- porphyria
- postpoliomyelitis syndrome
- postsurgical hypothyroidism
- primary coenzyme Q10 deficiency 1
- primary coenzyme Q10 deficiency 2
- primary coenzyme Q10 deficiency 5
- primary coenzyme Q10 deficiency 6
- primary coenzyme Q10 deficiency 7
- primary coenzyme Q10 deficiency 8
- primary coenzyme Q10 deficiency 9
- primary hyperaldosteronism
- primary hyperparathyroidism
- progressive relapsing multiple sclerosis
- proteasome-associated autoinflammatory syndrome 1
- radiculopathy
- reflex sympathetic dystrophy
- renal hypomagnesemia 2
- renal hypomagnesemia 7, with or without dilated cardiomyopathy
- renal osteodystrophy
- renal tubular transport disease
- rickets
- rigid spine muscular dystrophy 1
- scapuloperoneal spinal muscular atrophy
- secondary hyperparathyroidism
- sensory organ benign neoplasm
- skin disease
- spastic quadriplegic cerebral palsy 2
- spina bifida occulta
- spinal cancer
- spinal muscular atrophy
- spinal muscular atrophy with lower extremity predominant
- spinal muscular atrophy with lower extremity predominant 1
- spinal muscular atrophy with lower extremity predominant 2A
- spinal muscular atrophy, Jokela type
- spinal polio
- spinocerebellar ataxia 45
- spinocerebellar ataxia type 7
- spondyloepiphyseal dysplasia-brachydactyly and distinctive speech
- sporadic amyotrophic lateral sclerosis
- steroid inherited metabolic disorder
- stiff skin syndrome
- stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
- syphilis
- syringomyelia
- systemic primary carnitine deficiency disease
- thelaziasis
- thiamine deficiency disease
- thyroiditis
- thyrotoxicosis
- tibial muscular dystrophy
- tick paralysis
- transthyretin amyloidosis
- transverse myelitis
- trigeminal nerve neoplasm
- tropical spastic paraparesis
- variegate porphyria
- very long chain acyl-CoA dehydrogenase deficiency
- visual pathway disease
- vitamin B12 deficiency
- vitamin D-dependent rickets type 1A
- vitamin D-dependent rickets type 2B
- vitamin metabolic disorder
- xanthinuria type II
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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.