Disease Browser
Parent Node: Compartment Syndromes (D003161) Parent Node: Contracture (D003286) ..Starting node .. Ischemic Contracture (D054061) Child Nodes:
Sister Nodes: ..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) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 5923
Name: Ischemic Contracture
Definition: A type of permanent damage to muscles and nerves that results from prolonged lack blood flow to those tissues. It is characterized by shortening and stiffening of the muscles.
Alternative IDs:
ParentIDs: MESH:D003161|MESH:D003286
TreeNumbers: C05.550.323.734 |C05.651.180.531 |C05.651.197.734 |C14.907.303.531
Synonyms: Contracture, Ischemic |Contractures, Ischemic |Contractures, Volkmann |Contracture, Volkmann |Contracture, Volkmann's Ischemic |Ischemic Contractures |Ischemic Contracture, Volkmann's |Volkmann Contracture |Volkmann Contractures |Volkmann Ischemic Contracture |Vol
Slim Mappings: Cardiovascular disease|Musculoskeletal disease
Reference:
MedGen: D054061
MeSH: D054061
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants