Ontomatica – ChEMATIC (Wedge)

The current query selects 4071 items in 75 groups, which could be too many to show at once. If you are sure you want to see them all, you can proceed to see the entire category, 'or select a more specific subcategory of "Muscular Diseases [MESH:D009135]" below.

Subcategories in Musculoskeletal Diseases [MESH:D009140] > Muscular Diseases [MESH:D009135]:
(jump to A - C - D - E - F - H - I - K - M - N - O - P - R - S - T - U - V)

- A -
Alpha-B Crystallinopathy [MESH:C563848] (135)
Anal Sphincter Myopathy, Internal [MESH:C566287] (1)
Aplasia of Extensor Muscles of Fingers, Unilateral, with Generalized Polyneuropathy [MESH:C565945] (1)
Arthrogryposis [MESH:D001176] (329)

- C -
Camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia [MESH:C537974] (1)
Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)
Compartment Syndromes [MESH:D003161] (80)
Contracture [MESH:D003286] (303)
Craniomandibular Disorders [MESH:D017271] (33)

- D -
Dimauro disease [MESH:C536176] (33)

- E -
Encephalopathy, Axonal, with Necrotizing Myopathy, Cardiomyopathy, and Cataracts [MESH:C565596] (1)
Eosinophilia-Myalgia Syndrome [MESH:D016603] (31)
Epiphyseal Dysplasia, Multiple, with Myopathy [MESH:C563420] (1)
Erythrocyte Amp Deaminase Deficiency [MESH:C567878] (1)
Erythrocyte Lactate Transporter Defect [MESH:C565449] (106)

- F -
Fatigue Syndrome, Chronic [MESH:D015673] (3)
Fibromyalgia [MESH:D005356] (11)
Fingerprint Body Myopathy [MESH:C564425] (1)

- H -
Hereditary Myopathy with Early Respiratory Failure [MESH:C566343] (35)
Hypertrophia Musculorum Vera [MESH:C564152] (1)

- I -
Isaacs Syndrome [MESH:D020386] (5)

- K -
Kocher-Debre-Semelaigne syndrome [MESH:C537211] (1)

- M -
Marinesco-Sjogren-like syndrome (MSLS) [MESH:C535913] (1)
Medial Tibial Stress Syndrome [MESH:D058923] (1)
Mesoectodermal dysplasia [MESH:C538472] (1)
Mitochondrial DNA Depletion Syndrome, Myopathic Form [MESH:C563698] (1)
Mitochondrial Myopathies [MESH:D017240] (2176)
Muscle Cramp [MESH:D009120] (135)
Muscle Neoplasms [MESH:D019042] (3)
Muscle Rigidity [MESH:D009127] (617)
Muscle Spasticity [MESH:D009128] (187)
Muscle Weakness [MESH:D018908] (478)
Muscular Disorders, Atrophic [MESH:D020966] (1598)
Muscular Hypoplasia, Congenital Universal, of Krabbe [MESH:C563553] (1)
Musculoskeletal Pain [MESH:D059352] (1)
Myalgia [MESH:D063806] (1)
Myofascial Pain Syndromes [MESH:D009209] (9)
Myopathic carnitine deficiency [MESH:C536100] (1)
Myopathies, Structural, Congenital [MESH:D020914] (272)
Myopathy due to Malate-Aspartate Shuttle Defect [MESH:C564973] (1)
Myopathy with Giant Abnormal Mitochondria [MESH:C564971] (1)
Myopathy with Lactic Acidosis, Hereditary [MESH:C564972] (13)
Myopathy, Cataract, Hypogonadism Syndrome [MESH:C563578] (1)
Myopathy, Congenital, With Excess Of Muscle Spindles [MESH:C566896] (1)
Myopathy, Early-Onset, with Fatal Cardiomyopathy [MESH:C567129] (35)
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia [MESH:C564974] (1)
Myopathy, Hyaline Body, Autosomal Recessive [MESH:C564970] (1)
Myopathy, Myosin Storage [MESH:C564253] (77)
Myopathy, Reducing Body, X-Linked, Childhood-Onset [MESH:C567468] (64)
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe [MESH:C567469] (64)
Myopathy, X-Linked, with Excessive Autophagy [MESH:C564093] (6)
Myopathy, congenital nonprogressive with Moebius and Robin sequences [MESH:C536102] (1)
Myositis [MESH:D009220] (2071)
Myostatin-related muscle hypertrophy [MESH:C536106] (15)
Myotonic Disorders [MESH:D020967] (138)

- N -
Neutral Lipid Storage Disease with Myopathy [MESH:C565192] (58)

- O -
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria [MESH:C564925] (1)
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy [MESH:C565117] (1)

- P -
Paralyses, Familial Periodic [MESH:D010245] (57)
Pectoralis Muscle, Absence of [MESH:C566793] (1)
Polymyalgia Rheumatica [MESH:D011111] (3)
Proximal Myopathy with Focal Depletion of Mitochondria [MESH:C563453] (1)

- R -
Rhabdomyolysis [MESH:D012206] (465)
Rippling muscle disease, 1 [MESH:C535686] (31)

- S -
Salih Myopathy [MESH:C580430] (1)
Secretory Diarrhea, Myopathy, and Deafness [MESH:C564382] (1)
Singleton Merten syndrome [MESH:C537343] (1)
Systemic carnitine deficiency [MESH:C536778] (92)

- T -
Tel Hashomer camptodactyly syndrome [MESH:C536953] (1)
Tendinopathy [MESH:D052256] (14)
Treft Sanborn Carey syndrome [MESH:C536544] (1)
Triglyceride storage disease with impaired long-chain fatty acid oxidation [MESH:C536560] (31)

- U -
Uruguay Faciocardiomusculoskeletal Syndrome [MESH:C564544] (1)

- V -
VLCAD deficiency [MESH:C536353] (55)
Vacuolar myopathy [MESH:C536522] (5)