| Disease Browser
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Parent Node:
 Joint Diseases (D007592) |
Parent Node:
Muscular Diseases (D009135) |
..Starting node
.. Contracture (D003286)
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Child Nodes:
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| ........Aase Smith syndrome (C535332) |
| ........Alopecia contractures dwarfism mental retardation (C537051) |
| ........Arthropathy, Erosive (C565273) |
| ........Axial mesodermal dysplasia spectrum (C537790) |
| ........Bethlem myopathy (C535436) |
| ........Bone Fragility with Contractures, Arterial Rupture, and Deafness (C567320) |
| ........Bowen syndrome (C538164) |
| ........Camptodactyly joint contractures and facial skeletal dysplasia (C537969) |
| ........Congenital contractural arachnodactyly (C536211) |
| ........Congenital ectodermal dysplasia with hearing loss (C535757) |
| ........Contractures, Congenital, Torticollis, and Malignant Hyperthermia (C565679) |
| ........Davenport Donlan syndrome (C535988) |
........Dupuytren Contracture (D004387)  2 |
| ........Dystonia with Ringbinden (C565608) |
| ........Growth Deficiency and Mental Retardation with Facial Dysmorphism (C565358) |
| ........Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy (C564264) |
| ........Hip Contracture (D006616) |
| ........Histiocytosis with joint contractures and sensorineural deafness (C538322) |
| ........Iida Kannari syndrome (C536284) |
| ........Inclusion Body Myopathy 3, Autosomal Dominant (C565311) |
| ........Inclusion body myopathy, autosomal dominant (C538330) |
| ........Ischemic Contracture (D054061) |
| ........Lethal Congenital Contractural Syndrome 3 (C566961) |
| ........Macleod Fraser syndrome (C537715) |
| ........Marden Walker like syndrome (C535909) |
| ........Marden-Walker syndrome (C535910) |
| ........Mental retardation Mietens Weber type (C537444) |
| ........Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism (C565246) |
| ........Multiple Pterygium Syndrome, X-Linked (C564072) |
| ........Muscular dystrophy, tardive Emery-Dreifuss type, with contractures (C535734) |
| ........Muscular dystrophy, tardive, Dreifuss-Emery type, with contractures (C538478) |
| ........Rozin Hertz Goodman syndrome (C535876) |
| ........Spastic Paraplegia 18, Autosomal Recessive (C567628) |
| ........Spondylospinal Thoracic Dysostosis (C566622) |
| ........Stiff Skin Syndrome (C566112) |
| ........Tight skin contracture syndrome, lethal (C536920) |
| ........Wieacker syndrome (C536703) |
| ........Winchester syndrome (C536709) |
| ........Winter Harding Hyde syndrome (C536712) |
Sister Nodes: |
..Alpha-B Crystallinopathy (C563848)
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..Anal Sphincter Myopathy, Internal (C566287)
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..Aplasia of Extensor Muscles of Fingers, Unilateral, with Generalized Polyneuropathy (C565945)
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..Arthrogryposis (D001176) 55
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..Camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia (C537974)
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..Carnitine Palmitoyltransferase II Deficiency, Late-Onset (C563461)
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..Compartment Syndromes (D003161) 3
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..Contracture (D003286) 41
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..Craniomandibular Disorders (D017271) 4
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..Dimauro disease (C536176)
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..Encephalopathy, Axonal, with Necrotizing Myopathy, Cardiomyopathy, and Cataracts (C565596)
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..Eosinophilia-Myalgia Syndrome (D016603)
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..Epiphyseal Dysplasia, Multiple, with Myopathy (C563420)
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..Erythrocyte Amp Deaminase Deficiency (C567878)
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..Erythrocyte Lactate Transporter Defect (C565449)
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..Fatigue Syndrome, Chronic (D015673)
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..Fibromyalgia (D005356)
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..Fingerprint Body Myopathy (C564425)
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..Hereditary Myopathy with Early Respiratory Failure (C566343)
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..Hypertrophia Musculorum Vera (C564152)
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..Isaacs Syndrome (D020386)
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..Kocher-Debre-Semelaigne syndrome (C537211)
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..Marinesco-Sjogren-like syndrome (MSLS) (C535913)
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..Medial Tibial Stress Syndrome (D058923)
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..Mesoectodermal dysplasia (C538472)
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..Mitochondrial DNA Depletion Syndrome, Myopathic Form (C563698)
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..Mitochondrial Myopathies (D017240) 33
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..Muscle Cramp (D009120) 3
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..Muscle Neoplasms (D019042)
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..Muscle Rigidity (D009127) 3
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..Muscle Spasticity (D009128) 17
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..Muscle Weakness (D018908) 5
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..Muscular Disorders, Atrophic (D020966) 120
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..Muscular Hypoplasia, Congenital Universal, of Krabbe (C563553)
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..Musculoskeletal Pain (D059352) 2
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..Myalgia (D063806)
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..Myofascial Pain Syndromes (D009209) 1
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..Myopathic carnitine deficiency (C536100)
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..Myopathies, Structural, Congenital (D020914) 34
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..Myopathy due to Malate-Aspartate Shuttle Defect (C564973)
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..Myopathy with Giant Abnormal Mitochondria (C564971)
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..Myopathy with Lactic Acidosis, Hereditary (C564972)
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..Myopathy, Cataract, Hypogonadism Syndrome (C563578)
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..Myopathy, congenital nonprogressive with Moebius and Robin sequences (C536102)
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..Myopathy, Congenital, With Excess Of Muscle Spindles (C566896)
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..Myopathy, Early-Onset, with Fatal Cardiomyopathy (C567129)
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..Myopathy, Granulovacuolar Lobular, with Electrical Myotonia (C564974)
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..Myopathy, Hyaline Body, Autosomal Recessive (C564970)
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..MYOPATHY, MYOFIBRILLAR, 1 (OMIM:601419)
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..MYOPATHY, MYOFIBRILLAR, 4 (OMIM:609452)
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..MYOPATHY, MYOFIBRILLAR, 6 (OMIM:612954)
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..Myopathy, Myosin Storage (C564253)
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..Myopathy, Reducing Body, X-Linked, Childhood-Onset (C567468)
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..Myopathy, Reducing Body, X-Linked, Early-Onset, Severe (C567469)
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..Myopathy, X-Linked, with Excessive Autophagy (C564093)
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..Myositis (D009220) 16
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..Myostatin-related muscle hypertrophy (C536106)
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..Myotonic Disorders (D020967) 10
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..Neutral Lipid Storage Disease with Myopathy (C565192)
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..Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria (C564925)
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..Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy (C565117)
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..Paralyses, Familial Periodic (D010245) 7
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..Pectoralis Muscle, Absence of (C566793)
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..Polymyalgia Rheumatica (D011111)
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..Proximal Myopathy with Focal Depletion of Mitochondria (C563453)
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..Rhabdomyolysis (D012206) 6
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..Rippling muscle disease, 1 (C535686)
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..Salih Myopathy (C580430)
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..Secretory Diarrhea, Myopathy, and Deafness (C564382)
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..Singleton Merten syndrome (C537343)
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..Systemic carnitine deficiency (C536778)
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..Tel Hashomer camptodactyly syndrome (C536953)
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..Tendinopathy (D052256) 5
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..Treft Sanborn Carey syndrome (C536544)
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..Triglyceride storage disease with impaired long-chain fatty acid oxidation (C536560)
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..Uruguay Faciocardiomusculoskeletal Syndrome (C564544)
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..Vacuolar myopathy (C536522)
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..VLCAD deficiency (C536353)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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